Developmental Absence Of Tooth

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Results for "Developmental Absence Of Tooth": 30 genes, 1001 gene sets

Name
TST1 Gene Tuberculin skin test reactivity, absence* of*
ECA1 Gene epilepsy, childhood absence* 1*
LOC101060236 Gene developmental pluripotency associated 3 pseudogene
LOC100129344 Gene developmental pluripotency associated 4 pseudogene
DPPA3P2 Gene developmental pluripotency associated 3 pseudogene 2
DPPA3P1 Gene developmental pluripotency associated 3 pseudogene 1
IFRD1 Gene interferon-related developmental* regulator 1* This gene is an immediate early gene that encodes a protein related to interferon-gamma. This protein may function as a transcriptional co-activator/repressor that controls the growth and differentiation of specific cell types during embryonic development and tissue regeneration. Mutations in this gene are associated with sensory/motor neuropathy with ataxia. This gene may also be involved in modulating the pathogenesis of cystic fibrosis lung disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]
DPPA2P3 Gene developmental pluripotency associated 2 pseudogene 3
FENDRR Gene FOXF1 adjacent non-coding developmental* regulatory RNA* This gene produces a spliced long non-coding RNA transcribed bidirectionally with FOXF1 on the opposite strand. A similar gene in mouse is essential for normal development of the heart and body wall. The encoded transcript is thought to act by binding to polycomb repressive complex 2 (PRC2) and/or TrxG/MLL complexes to promote the methylation of the promoters of target genes, thus reducing their expression. It has been suggested that this transcript may play a role in the progression of gastric cancer. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
LOC100037267 Gene developmental pluripotency associated 4 pseudogene
DPPA2P1 Gene developmental pluripotency associated 2 pseudogene 1
DDH2 Gene Developmental dysplasia of the hip 2
DPPA5P4 Gene developmental pluripotency associated 5 pseudogene 4
DPPA5P1 Gene developmental pluripotency associated 5 pseudogene 1
DPPA5P3 Gene developmental pluripotency associated 5 pseudogene 3
DPPA5P2 Gene developmental pluripotency associated 5 pseudogene 2
DPPA2 Gene developmental pluripotency associated 2 Predicted to enable chromatin binding activity. Predicted to be involved in system development. Predicted to act upstream of or within several processes, including epigenetic regulation of gene expression; lung-associated mesenchyme development; and positive regulation of stem cell proliferation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]
DPPA3 Gene developmental pluripotency associated 3 This gene encodes a protein that in mice may function as a maternal factor during the preimplantation stage of development. In mice, this gene may play a role in transcriptional repression, cell division, and maintenance of cell pluripotentiality. In humans, related intronless loci are located on chromosomes 14 and X. [provided by RefSeq, Jul 2008]
DPPA4 Gene developmental pluripotency associated 4 This gene encodes a nuclear factor that is involved in the maintenance of pluripotency in stem cells and essential for embryogenesis. The encoded protein has a scaffold-attachment factor A/B, acinus and PIAS (SAP) domain that binds DNA and is thought to modify chromatin. Mice with a homozygous knockout of the orthologous gene die during late embryonic development or within hours after birth. Knockout embryos are normal in size at embryonic day 18.5 but exhibit skeletal and lung tissue abnormalities. This gene, when mutated, is highly expressed in embryonal carcinomas, pluripotent germ cell tumors, and other cancers and is thought to play an important role in tumor progression. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
DPPA5 Gene developmental pluripotency associated 5 This gene encodes a protein that may function in the control of cell pluripotency and early embryogenesis. Expression of this gene is a specific marker for pluripotent stem cells. Pseudogenes of this gene are located on the short arm of chromosome 10 and the long arm of chromosomes 14 and 19. [provided by RefSeq, Dec 2010]
DPPA4P1 Gene developmental pluripotency associated 4 pseudogene 1
LOC100130161 Gene developmental pluripotency associated 4 pseudogene
LOC100421154 Gene developmental pluripotency associated 4 pseudogene
LOC100421141 Gene developmental pluripotency associated 2 pseudogene
IFRD2 Gene interferon-related developmental* regulator 2* Enables ribosome binding activity and translation repressor activity. Involved in negative regulation of translation. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025]
LOC100421142 Gene developmental pluripotency associated 2 pseudogene
LOC100127919 Gene developmental pluripotency associated 3 pseudogene
DPPA2P2 Gene developmental pluripotency associated 2 pseudogene 2
DPPA2P4 Gene developmental pluripotency associated 2 pseudogene 4
SPACDR Gene sperm acrosome developmental* regulator* Involved in spermatid development. Located in acrosomal vesicle. [provided by Alliance of Genome Resources, Mar 2025]
Developmental Absence Of Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Absence Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
anodontia; developmental absence of tooth Gene Set From GAD Gene-Disease Associations genes associated with the disease anodontia; developmental absence of tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Primary tooth development (time to first tooth eruption) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Primary tooth development (time to first tooth eruption) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Partial congenital absence of teeth Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
(ER)-localized multiprotein complex, in absence of Ig heavy chains Gene Set From CORUM Protein Complexes proteins in the (ER)-localized multiprotein complex, in absence of Ig heavy chains protein complex from the CORUM Protein Complexes dataset.
Absence of Tibia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Absence of Tibia from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Absence Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Absence from the curated CTD Gene-Disease Associations dataset.
juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood absence epilepsy. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital bilateral absence of the vas deferens Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital bilateral absence of the vas deferens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
absence Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term absence in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2015 dataset.
absence of pectoralis minor muscle Gene Set From HPO Gene-Disease Associations genes associated with the absence of pectoralis minor muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital localized absence of skin Gene Set From HPO Gene-Disease Associations genes associated with the congenital localized absence of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of intrinsic factor Gene Set From HPO Gene-Disease Associations genes associated with the absence of intrinsic factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence seizures Gene Set From HPO Gene-Disease Associations genes associated with the absence seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of subcutaneous fat Gene Set From HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the absence of visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of bactericidal oxidative 'respiratory burst' in phagocytes Gene Set From HPO Gene-Disease Associations genes associated with the absence of bactericidal oxidative 'respiratory burst' in phagocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of lymph node germinal center Gene Set From HPO Gene-Disease Associations genes associated with the absence of lymph node germinal center phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of labia majora Gene Set From HPO Gene-Disease Associations genes associated with the absence of labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of secondary sex characteristics Gene Set From HPO Gene-Disease Associations genes associated with the absence of secondary sex characteristics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of subcutaneous fat over entire body except buttocks, hips, and thighs Gene Set From HPO Gene-Disease Associations genes associated with the absence of subcutaneous fat over entire body except buttocks, hips, and thighs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of pubertal development Gene Set From HPO Gene-Disease Associations genes associated with the absence of pubertal development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
deficiency or absence of cytochrome b(-245) Gene Set From HPO Gene-Disease Associations genes associated with the deficiency or absence of cytochrome b(-245) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of renal corticomedullary differentiation Gene Set From HPO Gene-Disease Associations genes associated with the absence of renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of cd8+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the absence of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial absence of thumb Gene Set From HPO Gene-Disease Associations genes associated with the partial absence of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of stensen duct Gene Set From HPO Gene-Disease Associations genes associated with the absence of stensen duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of acoustic reflex Gene Set From HPO Gene-Disease Associations genes associated with the absence of acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of lutheran antigen on erythrocytes Gene Set From HPO Gene-Disease Associations genes associated with the absence of lutheran antigen on erythrocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) Gene Set From HPO Gene-Disease Associations genes associated with the nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Epilepsy, Absence Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Absence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
absence of ampa-mediated synaptic currents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of ampa-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence of nmda-mediated synaptic currents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of nmda-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence of all nails Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence of all nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[tuberculin skin test reactivity, absence of] Gene Set From OMIM Gene-Disease Associations genes associated with the [tuberculin skin test reactivity, absence of] phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital bilateral absence of vas deferens Gene Set From OMIM Gene-Disease Associations genes associated with the congenital bilateral absence of vas deferens phenotype from the curated OMIM Gene-Disease Associations dataset.
ulna and fibula, absence of, with severe limb deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, childhood absence, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, juvenile absence, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, juvenile absence, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
Formation of HIV elongation complex in the absence of HIV Tat Gene Set From Reactome Pathways 2014 proteins participating in the Formation of HIV elongation complex in the absence of HIV Tat pathway from the Reactome Pathways dataset.
Abortive elongation of HIV-1 transcript in the absence of Tat Gene Set From Reactome Pathways 2014 proteins participating in the Abortive elongation of HIV-1 transcript in the absence of Tat pathway from the Reactome Pathways dataset.
Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Vas Deferens Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Spleen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Spleen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Muscle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Thymus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Germinal Epithelium Of Testes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Germinal Epithelium Of Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Kidneys Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Kidneys Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Septum Pellucidum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Septum Pellucidum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Both Testes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Both Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Parathyroid Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Parathyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Localized Absence Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Localized Absence Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Seizure Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Seizure Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of External Ear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Mandible Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Mandible in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Lung Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Unilateral Absence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Unilateral Absence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Absence Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Absence Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Tibia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Tibia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lacrimal Puncta, Absence Of Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Puncta, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Bladder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Uvula Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Alpha Granules Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Alpha Granules in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Jaw Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Jaw in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Diaphragm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Diaphragm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Lutheran Antigen On Erythrocytes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Lutheran Antigen On Erythrocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Of Tibia With Polydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absence Of Tibia With Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Absence Of Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Absence Of Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Breast With Absent Nipple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Breast With Absent Nipple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Penis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Penis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence, Atresia And Stricture Of Auditory Canal (External) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence, Atresia And Stricture Of Auditory Canal (External) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Part Of Brain Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Part Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Pulmonic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Pulmonic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atonic Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atonic Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Lymph Node Germinal Center Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Lymph Node Germinal Center in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pubertal Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pubertal Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Secondary Sex Characteristics Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Secondary Sex Characteristics in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Typical Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Typical Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Rib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Rib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Subcutaneous Fat Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Subcutaneous Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Intrinsic Factor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Intrinsic Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Cd8-Positive T Cells Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Cd8-Positive T Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vas Deferens, Congenital Bilarteral, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vas Deferens, Congenital Bilarteral, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Labia Majora Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Labia Majora in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stomach Bubble On Fetal Sonography Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stomach Bubble On Fetal Sonography in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fingerprints, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fingerprints, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Bactericidal Oxidative Respiratory Burst In Phagocytes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Bactericidal Oxidative Respiratory Burst In Phagocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Deficiency Or Absence Of Cytochrome B(-245) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deficiency Or Absence Of Cytochrome B(-245) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pain Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Acoustic Reflex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Acoustic Reflex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Attacks Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Attacks in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stensen Duct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stensen Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Islets Of Langerhans, Absence Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Islets Of Langerhans, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Absence Of Foot Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Absence Of Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Renal Corticomedullary Differentiation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Renal Corticomedullary Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Pectoralis Minor Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pectoralis Minor Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Absence Of Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Absence Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2023 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2023 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2023 dataset.
absence seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of NMDA-mediated synaptic currents Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of NMDA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of all nails Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of all nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence of AMPA-mediated synaptic currents Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence of AMPA-mediated synaptic currents phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Abortive elongation of HIV-1 transcript in the absence of Tat Gene Set From Reactome Pathways 2024 proteins participating in the Abortive elongation of HIV-1 transcript in the absence of Tat pathway from the Reactome Pathways 2024 dataset.
Caspase activation via Dependence Receptors in the absence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the Caspase activation via Dependence Receptors in the absence of ligand pathway from the Reactome Pathways 2024 dataset.
Formation of HIV elongation complex in the absence of HIV Tat Gene Set From Reactome Pathways 2024 proteins participating in the Formation of HIV elongation complex in the absence of HIV Tat pathway from the Reactome Pathways 2024 dataset.
negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
collateral sprouting in absence of injury Gene Set From GO Biological Process Annotations 2025 genes participating in the collateral sprouting in absence of injury biological process from the curated GO Biological Process Annotations 2025 dataset.
extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of signal transduction in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of signal transduction in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of extrinsic apoptotic signaling pathway in absence of ligand biological process from the curated GO Biological Process Annotations 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bilateral absence of vas deferens from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bilateral absence of vas deferens in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked congenital bilateral absence of vas deferens Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked congenital bilateral absence of vas deferens in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile absence epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile absence epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Absence of the sacrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Absence of the sacrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital bilateral absence of vas deferens Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral absence of vas deferens phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Typical absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Typical absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic absence seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic absence seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEVELOPMENTAL DYSPLASIA OF THE HIP 1 from the curated CTD Gene-Disease Associations dataset.
Developmental Disabilities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Developmental Disabilities from the curated CTD Gene-Disease Associations dataset.
Bone Diseases, Developmental Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Developmental from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pervasive developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease specific developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bone diseases, developmental; osteoarthritis, hip Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases, developmental; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
developmental Gene Set From GAD High Level Gene-Disease Associations genes associated with the disease developmental in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
developmental Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term developmental in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
developmental maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental growth involved in morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental growth involved in morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
single-organism developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the single-organism developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental cell growth Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental cell growth biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
pigment metabolic process involved in developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the pigment metabolic process involved in developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental induction Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental induction biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental process involved in reproduction Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental process involved in reproduction biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental process Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental process biological process from the curated GO Biological Process Annotations 2015 dataset.
spongiotrophoblast layer developmental growth Gene Set From GO Biological Process Annotations 2015 genes participating in the spongiotrophoblast layer developmental growth biological process from the curated GO Biological Process Annotations 2015 dataset.
specific developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease specific developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental disorder of mental health Gene Set From GWASdb SNP-Disease Associations genes associated with the disease developmental disorder of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
pervasive developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease pervasive developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental stagnation Gene Set From HPO Gene-Disease Associations genes associated with the developmental stagnation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
moderate global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the moderate global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
developmental stagnation at onset of seizures Gene Set From HPO Gene-Disease Associations genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
developmental regression Gene Set From HPO Gene-Disease Associations genes associated with the developmental regression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Developmental Disabilities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Developmental Disabilities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bone Diseases, Developmental Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bone Diseases, Developmental phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Developmental pluripotency-associated protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sox developmental protein N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sox developmental protein N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interferon-related developmental regulator, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon-related developmental regulator, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interferon-related developmental regulator, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon-related developmental regulator, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal developmental patterning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal developmental patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal developmental vascular remodeling Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal developmental vascular remodeling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
developmental dysplasia of the hip 2 Gene Set From OMIM Gene-Disease Associations genes associated with the developmental dysplasia of the hip 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, hyperphagia, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, seizures, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, seizures, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
?obesity, hyperphagia, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the ?obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation, developmental delay, coarse facies, and early death Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.
sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
developmental Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term developmental in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Developmental Biology Gene Set From Reactome Pathways 2014 proteins participating in the Developmental Biology pathway from the Reactome Pathways dataset.
Developmental Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Global Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Coordination Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Coordination Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Reading Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Reading Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Global Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Arithmetic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Arithmetic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brachycephaly, Trichomegaly, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brachycephaly, Trichomegaly, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intellectual Developmental Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intellectual Developmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phonological Developmental Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phonological Developmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lateral Developmental Cyst Of Jaw Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lateral Developmental Cyst Of Jaw in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Porencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Porencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Failure Of Fusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Failure Of Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Coxa Vara Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Coxa Vara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Communication Disorders, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Communication Disorders, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Dysplasia Of The Hip 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Dysplasia Of The Hip 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Valvular Defect, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Syntactic Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Syntactic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental And Speech Delay Due To Sox5 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental And Speech Delay Due To Sox5 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Plantar Lipomatosis, Unusual Facies, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plantar Lipomatosis, Unusual Facies, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac, Facial, And Digital Anomalies With Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac, Facial, And Digital Anomalies With Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay (Disorder) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Stagnation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Stagnation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Academic Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Academic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderate Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Stagnation At Onset Of Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Stagnation At Onset Of Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pili Torti Developmental Delay Neurological Abnormalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pili Torti Developmental Delay Neurological Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Delay, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Developmental Milestones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Developmental Milestones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal developmental patterning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal developmental patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
developmental cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the developmental cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal developmental vascular remodeling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal developmental vascular remodeling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
behavioral developmental delay Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the behavioral developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor developmental delay Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Developmental Biology Gene Set From Reactome Pathways 2024 proteins participating in the Developmental Biology pathway from the Reactome Pathways 2024 dataset.
Developmental Cell Lineages Gene Set From Reactome Pathways 2024 proteins participating in the Developmental Cell Lineages pathway from the Reactome Pathways 2024 dataset.
Disorders of Developmental Biology Gene Set From Reactome Pathways 2024 proteins participating in the Disorders of Developmental Biology pathway from the Reactome Pathways 2024 dataset.
Pervasive developmental disorders Gene Set From Reactome Pathways 2024 proteins participating in the Pervasive developmental disorders pathway from the Reactome Pathways 2024 dataset.
positive regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of developmental growth Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of developmental growth biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of developmental process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of developmental process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of developmental process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of developmental pigmentation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of developmental pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental disorder of mental health from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pervasive developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Specific developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 14 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 29 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 13 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease microcephaly, seizures, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 26 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked intellectual developmental disorder 109 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 43 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 86 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 86 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease microcephaly, seizures, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental dysplasia of the hip Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental dysplasia of the hip 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental dysplasia of the hip 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental dysplasia of the hip 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 80 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 80 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 93 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 93 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 53 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 53 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay and seizures with or without movement abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with short stature and behavioral abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with short stature and behavioral abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 98 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 98 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 108 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 108 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital limbs-face contractures-hypotonia-developmental delay syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with cardiac arrhythmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with cardiac arrhythmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 31A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 31A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 60 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 60 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 62 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 62 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 103 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 103 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 91 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 91 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 66 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 66 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 109 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 94 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 94 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 6B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 6B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 65 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 65 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental cardiac valvular defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual developmental disorder bain type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual developmental disorder bain type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 97 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 97 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 102 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 102 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
brachycephaly, trichomegaly, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease brachycephaly, trichomegaly, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 59 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 59 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 67 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 67 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 104 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 104 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 106 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 106 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 74 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 74 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 58 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 58 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 90 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 90 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual developmental disorder 111 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual developmental disorder 111 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 72 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 72 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 71 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 71 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 100 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 100 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 96 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 96 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 89 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 89 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with ocular anomalies and distinctive facial features Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with ocular anomalies and distinctive facial features in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay, hypotonia, and impaired language Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay, hypotonia, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiac anomalies - developmental delay - facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac anomalies - developmental delay - facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental regression Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental regression phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe achondroplasia-developmental delay-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental malformations-deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental malformations-deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
INTELLECTUAL DEVELOPMENTAL DISOR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the INTELLECTUAL DEVELOPMENTAL DISOR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental delay and seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental delay and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocephaly-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocephaly-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancytopenia-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancytopenia-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Genetic developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related Autism and developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related Autism and developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Moderate global developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Moderate global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNAO1-related developmental delay-seizures-movement disorder spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-brachydactyly-obesity-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-brachydactyly-obesity-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Unclassified developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Unclassified developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BSCL2-related Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BSCL2-related Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Noonan Syndrome-like developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan Syndrome-like developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder and retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder and retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pervasive developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pervasive developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental dysplasia of the hip Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental dysplasia of the hip phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder- Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder- phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HCN2 related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HCN2 related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SNAP25-related early-onset developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SNAP25-related early-onset developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pili torti-developmental delay-neurological abnormalities syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pili torti-developmental delay-neurological abnormalities syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SEPHS1-related developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SEPHS1-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pubertal developmental failure in females Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pubertal developmental failure in females phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GRIN2B-related developmental delay Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GRIN2B-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
USP9X-related intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the USP9X-related intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FRYL-related developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FRYL-related developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNA3-associated developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNA3-associated developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GABRA4-related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GABRA4-related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental language disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Developmental language disorder (linguistic errors) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder (linguistic errors) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Developmental language disorder (syntactic complexity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental language disorder (syntactic complexity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Developmental dysplasia of the hip Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Developmental dysplasia of the hip phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IVF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Failure of tooth eruption, primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Failure of tooth eruption, primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2A1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type ID Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IB Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tooth agenesis, selective, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tooth agenesis, selective, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tooth agenesis, selective, X-linked, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tooth agenesis, selective, X-linked, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate d Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate c Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tooth agenesis, selective, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tooth agenesis, selective, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tooth agenesis, selective, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tooth agenesis, selective, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2M Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, Type 2K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset.
Tooth Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Abnormalities from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.
Tooth Agenesis, Selective, X-Linked, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Agenesis, Selective, X-Linked, 1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.
Tooth Loss Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Loss from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Type 4j Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset.
Failure of Tooth Eruption, Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Failure of Tooth Eruption, Primary from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.
Tooth Agenesis, Selective, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Agenesis, Selective, 5 from the curated CTD Gene-Disease Associations dataset.
Tooth Agenesis, Selective, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Agenesis, Selective, 6 from the curated CTD Gene-Disease Associations dataset.
Tooth Agenesis, Selective, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Agenesis, Selective, 3 from the curated CTD Gene-Disease Associations dataset.
Tooth Agenesis, Selective, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Agenesis, Selective, 2 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Type 4H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.
Tooth Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Injuries from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B2 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4B1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4B2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B2 from the curated CTD Gene-Disease Associations dataset.
Tooth Eruption Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Tooth Eruption in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
tooth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease tooth disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease charcot-marie-tooth disease type 3 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease charcot-marie-tooth disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
tooth disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease tooth disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
tooth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth and nail syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth and nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth ankylosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth ankylosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth erosion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type x Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease type x in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
charcot-marie-tooth disease type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease charcot-marie-tooth disease type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth resorption Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth resorption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth agenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth agenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
clinically distinct charcot-marie-tooth phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease clinically distinct charcot-marie-tooth phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy type 1b Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth neuropathy type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; periodontitis; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth, edentulous; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal recessive charcot-marie-tooth disease Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal recessive charcot-marie-tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, charcot-marie-tooth Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, charcot-marie-tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary tooth development Gene Set From GAD Gene-Disease Associations genes associated with the disease primary tooth development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recessive charcot-marie-tooth disease Gene Set From GAD Gene-Disease Associations genes associated with the disease recessive charcot-marie-tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth type 1b Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
x-linked charcot-marie tooth disease Gene Set From GAD Gene-Disease Associations genes associated with the disease x-linked charcot-marie tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; periodontal attachment loss; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; genetic diseases, x-linked Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth type 1 disease Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth type 1 disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease type 1a Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease type 1a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease type 1b Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; tooth abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; tooth abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival crevicular fluid and orthodontic tooth movement Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival crevicular fluid and orthodontic tooth movement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tooth eruption Gene Set From GAD Gene-Disease Associations genes associated with the disease tooth eruption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tooth Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term tooth in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2015 dataset.
tooth mineralization Gene Set From GO Biological Process Annotations 2015 genes participating in the tooth mineralization biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2015 dataset.
odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2015 genes participating in the odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2015 dataset.
tooth eruption Gene Set From GO Biological Process Annotations 2015 genes participating in the tooth eruption biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2015 dataset.
structural constituent of tooth enamel Gene Set From GO Molecular Function Annotations 2015 genes performing the structural constituent of tooth enamel molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Tooth agenesis (third molar) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Tooth agenesis (third molar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Primary tooth development (number of teeth) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Primary tooth development (number of teeth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Permanent tooth development Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Permanent tooth development phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
tooth disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease tooth disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
tooth agenesis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease tooth agenesis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
selective tooth agenesis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the selective tooth agenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
unerupted tooth Gene Set From HPO Gene-Disease Associations genes associated with the unerupted tooth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
natal tooth Gene Set From HPO Gene-Disease Associations genes associated with the natal tooth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
molar tooth sign on mri Gene Set From HPO Gene-Disease Associations genes associated with the molar tooth sign on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
double tooth Gene Set From HPO Gene-Disease Associations genes associated with the double tooth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impacted tooth Gene Set From HPO Gene-Disease Associations genes associated with the impacted tooth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
selective tooth agenesis Gene Set From HPO Gene-Disease Associations genes associated with the selective tooth agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
conical tooth Gene Set From HPO Gene-Disease Associations genes associated with the conical tooth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Tooth Abnormalities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth Loss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth Demineralization Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Demineralization phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth, Supernumerary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth, Supernumerary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth, Nonvital Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth, Nonvital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tooth Mobility Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Mobility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal tooth morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent tooth primordium Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent tooth primordium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth mineralization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth mineralization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth hard tissue morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth hard tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
embryonic lethality prior to tooth bud stage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the embryonic lethality prior to tooth bud stage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
arrest of tooth development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the arrest of tooth development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth eruption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth root development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth root development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed tooth eruption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth color Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of tooth eruption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
accelerated tooth eruption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the accelerated tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis Gene Set From OMIM Gene-Disease Associations genes associated with the dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate e Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate e phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate c Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate c phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate b Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate b phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, dominant intermediate a Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, dominant intermediate a phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, type 2r Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, x-linked dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, x-linked dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, x-linked recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, x-linked recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, recessive intermediate, a Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, recessive intermediate, a phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2a1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2a1 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2a2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2a2 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, foot deformity of Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, foot deformity of phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1c Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 1a Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
failure of tooth eruption, primary Gene Set From OMIM Gene-Disease Associations genes associated with the failure of tooth eruption, primary phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, recessive intermediate d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, recessive intermediate d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, recessive intermediate c Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, recessive intermediate c phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, type 4b3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, type 4b3 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, x-linked 1 Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 1, with or without orofacial cleft Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4b2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4b2 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4b1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4b1 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, recessive intermediate, b Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, recessive intermediate, b phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2k Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2k phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2n Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2n phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2m Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2m phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 20 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia 8, hair/tooth/nail type Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2b1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2b1 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2b2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2b2 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2e Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2j Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 2i Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 2i phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, axonal, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, axonal, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4h Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4h phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4j Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4j phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4a Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4c Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4c phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4d Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4d phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, type 4f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, type 4f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, with vocal cord paresis Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, with vocal cord paresis phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth bud Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue tooth bud from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
tooth Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue tooth from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
tooth enamel Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tooth enamel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
tooth Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tooth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
tooth bud Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tooth bud in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
tooth germ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tooth germ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Charcot-Marie-Tooth Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Charcot-Marie-Tooth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Attrition Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Attrition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Charcot-Marie-Tooth Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Charcot-Marie-Tooth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Disturbances In Tooth Structure, Not Elsewhere Classified In Icd10Cm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Disturbances In Tooth Structure, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Agenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Development And Eruption Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Development And Eruption Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supernumerary Mesiodens Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supernumerary Mesiodens Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ectopic Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomineralization Of Enamel Of Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomineralization Of Enamel Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Failure Of Tooth Eruption, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Failure Of Tooth Eruption, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periapical Tooth Abscess Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periapical Tooth Abscess in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nail And Tooth Abnormalities, Marginal Palmoplantar Keratoderma, Oral Hyperpigmentation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nail And Tooth Abnormalities, Marginal Palmoplantar Keratoderma, Oral Hyperpigmentation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Resorption Of Apex Of Tooth Root Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Resorption Of Apex Of Tooth Root in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Failure Of Tooth Eruption Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Failure Of Tooth Eruption in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Ankylosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Ankylosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
External Resorption Of Tooth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease External Resorption Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Surf1-Related Charcot-Marie-Tooth Disease Type 4 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surf1-Related Charcot-Marie-Tooth Disease Type 4 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Eruption Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Eruption Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Disturbances In Tooth Structure, Nec In Icd9Cm_2014 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Disturbances In Tooth Structure, Nec In Icd9Cm_2014 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Tooth Eruption Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late Tooth Eruption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tooth Crowding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tooth Crowding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tooth, Supernumerary Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tooth, Supernumerary in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Premature Tooth Eruption Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Tooth Eruption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Molar Tooth Sign On Mri Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Molar Tooth Sign On Mri in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Precocious Exfoliation Of Primary Tooth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Precocious Exfoliation Of Primary Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unerupted Tooth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unerupted Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tooth Absent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tooth Absent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Selective Tooth Agenesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Selective Tooth Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Failure Of Exfoliation Of Primary Tooth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Failure Of Exfoliation Of Primary Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tooth Agenesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tooth Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Premature Tooth Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Tooth Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Charcot-Marie-Tooth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Microcephalic Osteodysplastic Primordial Dwarfism With Tooth Abnormalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Microcephalic Osteodysplastic Primordial Dwarfism With Tooth Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2023 genes participating in the odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2023 dataset.
tooth mineralization Gene Set From GO Biological Process Annotations 2023 genes participating in the tooth mineralization biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2023 dataset.
structural constituent of tooth enamel Gene Set From GO Molecular Function Annotations 2023 genes performing the structural constituent of tooth enamel molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal tooth development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth mineralization Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth mineralization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
arrest of tooth development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the arrest of tooth development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth eruption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth eruption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of tooth eruption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of tooth eruption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed tooth eruption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed tooth eruption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent tooth placode Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent tooth placode phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth hard tissue morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth hard tissue morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth attrition Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth attrition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature tooth eruption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature tooth eruption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased tooth number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tooth number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth root resorption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth root resorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth wear Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth wear phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
tooth impaction Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the tooth impaction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth color Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth color phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short tooth root Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short tooth root phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth root development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth root development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
apical tooth abscess Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the apical tooth abscess phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth root morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth root morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality prior to tooth bud stage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality prior to tooth bud stage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality prior to tooth bud stage, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality prior to tooth bud stage, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality prior to tooth bud stage Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the embryonic lethality prior to tooth bud stage phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal tooth morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal tooth morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal tooth color Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal tooth color phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Tooth progenitor cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Tooth progenitor cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
OSX and miRNAs in tooth development Gene Set From WikiPathways Pathways 2024 proteins participating in the OSX and miRNAs in tooth development pathway from the WikiPathways Pathways 2024 dataset.
odontogenesis of dentin-containing tooth Gene Set From GO Biological Process Annotations 2025 genes participating in the odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations 2025 dataset.
tooth mineralization Gene Set From GO Biological Process Annotations 2025 genes participating in the tooth mineralization biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of tooth mineralization Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of tooth mineralization biological process from the curated GO Biological Process Annotations 2025 dataset.
structural constituent of tooth enamel Gene Set From GO Molecular Function Annotations 2025 genes performing the structural constituent of tooth enamel molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Charcot-Marie-Tooth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Charcot-Marie-Tooth disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Charcot-Marie-Tooth disease type 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Tooth disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Tooth disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Tooth disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Tooth disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth agenesis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Tooth agenesis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth agenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth agenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary failure of tooth eruption Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary failure of tooth eruption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth ankylosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth ankylosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease, axonal type 2W Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease, axonal type 2W in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth resorption Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth resorption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth erosion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2EE Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2EE in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked recessive 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked recessive 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type X Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type X in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2Y Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2Y in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease recessive intermediate D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease recessive intermediate D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked recessive 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked recessive 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2Q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4B1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4B3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2B1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease recessive intermediate B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease recessive intermediate B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease intermediate type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease intermediate type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2A2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2A2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked dominant 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2A2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2A2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2DD Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2DD in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked dominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2A1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2A1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2Z Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2Z in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2S Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2S in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2T Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2R Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2R in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2P Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2P in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2CC Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2CC in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease recessive intermediate C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease recessive intermediate C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 1F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 1F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 2J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 2J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2U Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2U in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked recessive 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked recessive 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease recessive intermediate A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease recessive intermediate A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2V Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2V in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth and nail syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tooth and nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2N Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2N in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease dominant intermediate F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2O Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease X-linked recessive 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease X-linked recessive 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tooth bud Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Tooth bud from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Tooth Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Tooth from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Tooth enamel Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tooth enamel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Tooth germ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tooth germ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Tooth Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tooth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Tooth bud Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tooth bud in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Pharyngeal tooth Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pharyngeal tooth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease dominant intermediate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease dominant intermediate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease axonal Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease axonal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Molar tooth sign on Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Molar tooth sign on phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease recessive intermediate Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease recessive intermediate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease X-linked recessive Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease X-linked dominant Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease X-linked dominant phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary failure of tooth eruption Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary failure of tooth eruption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CHARCOT-MARIE-TOOTH DISE Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CHARCOT-MARIE-TOOTH DISE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant intermediate Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant intermediate Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Selective tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Selective tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TSPEAR-related disorder of tooth and hair follicle morphogenesis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TSPEAR-related disorder of tooth and hair follicle morphogenesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease axonal - Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease axonal - phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MME-related autosomal dominant Charcot Marie Tooth disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MME-related autosomal dominant Charcot Marie Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tooth agenesis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Tooth agenesis (mandibular second premolars) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (mandibular second premolars) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Tooth agenesis (maxillary lateral incisors) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (maxillary lateral incisors) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Tooth agenesis (maxillary second premolars) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (maxillary second premolars) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Tooth agenesis (third molar) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Tooth agenesis (third molar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

TST1 Gene

ECA1 Gene

LOC101060236 Gene

LOC100129344 Gene

DPPA3P2 Gene

DPPA3P1 Gene

IFRD1 Gene

DPPA2P3 Gene

FENDRR Gene

LOC100037267 Gene

DPPA2P1 Gene

DDH2 Gene

DPPA5P4 Gene

DPPA5P1 Gene

DPPA5P3 Gene

DPPA5P2 Gene

DPPA2 Gene

DPPA3 Gene

DPPA4 Gene

DPPA5 Gene

DPPA4P1 Gene

LOC100130161 Gene

LOC100421154 Gene

LOC100421141 Gene

IFRD2 Gene

LOC100421142 Gene

LOC100127919 Gene

DPPA2P2 Gene

DPPA2P4 Gene

SPACDR Gene

Developmental Absence Of Tooth Gene Set

anodontia; developmental absence of tooth Gene Set

Primary tooth development (time to first tooth eruption) Gene Set

Primary tooth development (time to first tooth eruption) Gene Set

Congenital absence of salivary gland Gene Set

Ulna and fibula absence of with severe limb deficiency Gene Set

Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set

Partial congenital absence of teeth Gene Set

(ER)-localized multiprotein complex, in absence of Ig heavy chains Gene Set

Absence of Tibia Gene Set

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

Epilepsy, Absence Gene Set

juvenile absence epilepsy Gene Set

childhood absence epilepsy Gene Set

early onset absence epilepsy Gene Set

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

childhood absence epilepsy. Gene Set

epilepsy, absence; epilepsy, generalized Gene Set

congenital bilateral absence of the vas deferens Gene Set

absence Gene Set

positive regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

positive regulation of collateral sprouting in absence of injury Gene Set

extrinsic apoptotic signaling pathway in absence of ligand Gene Set

collateral sprouting in absence of injury Gene Set

regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

signal transduction in absence of ligand Gene Set

negative regulation of extrinsic apoptotic signaling pathway in absence of ligand Gene Set

negative regulation of collateral sprouting in absence of injury Gene Set

regulation of collateral sprouting in absence of injury Gene Set

negative regulation of signal transduction in absence of ligand Gene Set

absence of pectoralis minor muscle Gene Set

congenital localized absence of skin Gene Set

absence of intrinsic factor Gene Set

absence seizures Gene Set

absence of subcutaneous fat Gene Set

absence of visual evoked potentials Gene Set

absence of bactericidal oxidative 'respiratory burst' in phagocytes Gene Set

absence of lymph node germinal center Gene Set

absence of labia majora Gene Set

absence of secondary sex characteristics Gene Set

absence of subcutaneous fat over entire body except buttocks, hips, and thighs Gene Set

absence of pubertal development Gene Set

deficiency or absence of cytochrome b(-245) Gene Set

absence of renal corticomedullary differentiation Gene Set

absence of cd8+ t cells Gene Set

partial absence of thumb Gene Set

absence of stensen duct Gene Set

absence of acoustic reflex Gene Set

absence of lutheran antigen on erythrocytes Gene Set