Filters:

Results for "Absence of labia majora": 2 genes, 186 gene sets

Name

TST1 Gene

Tuberculin skin test reactivity, absence of

ECA1 Gene

epilepsy, childhood absence 1

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 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.

abnormality of the labia majora Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic labia majora Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Abnormality Of The Labia Majora Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of The Labia Majora in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Labia Majora Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Small Labia Majora in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormality of the labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fused labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the fused labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypertrophic labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the hypertrophic labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

enlarged labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the enlarged labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the labia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Abnormality Of The Labia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of The Labia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fused Labia Minora Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fused Labia Minora in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Enlarged Labia Minora Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Enlarged Labia Minora in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations 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.

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.

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 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.

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.

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 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.