| Name |
|---|
TAM GeneMyeloproliferative syndrome, transient (transient abnormal |
ASPM Geneasp (abnormal spindle) homolog, microcephaly associated (Drosophila) This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011] |
MNDEC GeneMicrotia with nasolacrimal duct imperforation and eye coloboma |
CECR5 Genecat eye syndrome chromosome region, candidate 5 Predicted to be involved in glycerophospholipid biosynthetic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
CECR9 Genecat eye syndrome chromosome region, candidate 9 (non-protein coding) Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
BED GeneBornholm eye disease |
OED GeneOregon eye disease |
CECR1 Genecat eye syndrome chromosome region, candidate 1 This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
CECR2 Genecat eye syndrome chromosome region, candidate 2 This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
CECR3 Genecat eye syndrome chromosome region, candidate 3 (non-protein coding) |
CECR6 Genecat eye syndrome chromosome region, candidate 6 |
EYCL1 Geneeye color 1 (green/blue) |
SHEP8 GeneSkin/hair/eye pigmentation 8, freckling |
CECR7 Genecat eye syndrome chromosome region, candidate 7 (non-protein coding) |
CECR Genecat eye syndrome chromosome region Cat eye syndrome (CES) is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. A small supernumerary chromosome (smaller than chromosome 21) is present, frequently has 2 centromeres, is bisatellited, and represents an inv dup(22)(q11).[supplied by OMIM, Aug 2009] |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Eye Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Eye Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal eye physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye neoplasms; melanoma; tumour of eye Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye neoplasms; melanoma; tumour of eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Eye-eye photoreceptor cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-eye photoreceptor cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal submandibular gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thymus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuronal stem cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hearing physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hearing physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, alpha-beta t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, alpha-beta t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory epithelium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory epithelium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oligodendrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oligodendrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 1 physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 1 physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adrenal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sex gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sex gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal professional antigen presenting cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal professional antigen presenting cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hematopoietic system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hematopoietic stem cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic stem cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal autonomic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sweat gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sweat gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd8-positive, alpha-beta t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, alpha-beta t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ependyma motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal extraembryonic tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal extraembryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal harderian gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal harderian gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lysosome physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lysosome physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal astrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal astrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic delta cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic delta cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland epithelium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland epithelium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal muscle precursor cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal muscle precursor cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cytotoxic t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cytotoxic t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eosinophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eosinophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeleton physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeleton physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nonmotile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nonmotile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visceral endoderm physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visceral endoderm physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal germinal center b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal germinal center b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile duct physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cardiac valve physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiac valve physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal follicular dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal follicular dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t follicular helper cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t follicular helper cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatobiliary system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatobiliary system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 2 physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 2 physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oval cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oval cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal langerhans cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal langerhans cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal carotid body physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal carotid body physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal podocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal podocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal salivary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal salivary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin adnexa physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin adnexa physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine nk cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine nk cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gustatory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gustatory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pineal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pineal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphatic system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphatic system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestinal crypt cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cardiovascular system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiovascular system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal microglial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal microglial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parathyroid gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parathyroid gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mast cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mast cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune serum protein physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune serum protein physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal granulocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal granulocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal histamine physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal histamine physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myocardial fiber physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myocardial fiber physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood vessel physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoclast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoclast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal marginal zone b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal marginal zone b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic nervous system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal erythrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal erythrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pre-botzinger complex physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pre-botzinger complex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal follicular b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal follicular b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sebaceous gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sebaceous gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet dense granule physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet dense granule physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sperm physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sperm physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal/urinary system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal/urinary system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gabaergic neuron physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gabaergic neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung endothelial cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung endothelial cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic beta cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic beta cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nk cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nk cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal muscle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal muscle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal leukocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal regulatory t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal regulatory t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal baroreceptor physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal baroreceptor physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ureter physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ureter physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory b cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory b cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic alpha cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic alpha cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular smooth muscle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular smooth muscle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nk t cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nk t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oviduct physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oviduct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal cardiomyocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pp cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pp cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gastroesophageal sphincter physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gastroesophageal sphincter physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 17 cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 17 cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hypothalamus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune organ physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune organ physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chondrocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chondrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiratory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Aortic Valve Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Mitral Valve Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Mitral Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Large Intestine Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Large Intestine Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Bronchus Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Bronchus Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Lymphocyte Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lymphocyte Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Hypothalamus Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Hypothalamus Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Natural Killer Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Natural Killer Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thymus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thymus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal digestive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal digestive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal muscle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal muscle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ear physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ear physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adrenal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adrenal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal osteoclast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal osteoclast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hearing physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hearing physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skeleton physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeleton physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal salivary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal salivary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal macrophage physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal macrophage physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 1 physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 1 physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 2 physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 2 physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vascular smooth muscle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular smooth muscle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mitochondrial physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neutrophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neutrophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cardiovascular system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiovascular system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Langerhans cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Langerhans cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood vessel physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymphocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymphocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal follicular dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal follicular dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cytotoxic T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cytotoxic T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal prostate gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bulbourethral gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bulbourethral gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sympathetic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sympathetic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatobiliary system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatobiliary system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal microglial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal microglial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hematopoietic stem cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hematopoietic stem cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sperm physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal CD4-positive, alpha-beta T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal CD4-positive, alpha-beta T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal platelet physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal platelet physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal erythrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal erythrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestine physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal small intestinal crypt cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal keratinocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic beta cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic beta cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal extraembryonic tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extraembryonic tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal astrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal astrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal NK cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal NK cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skin physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skin physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal leukocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal myocardial fiber physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal myocardial fiber physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immune serum protein physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immune serum protein physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal osteoblast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal professional antigen presenting cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal professional antigen presenting cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mast cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mast cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal baroreceptor physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal baroreceptor physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hematopoietic system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hematopoietic system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal uterus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gallbladder physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gallbladder physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal spleen physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pre-Botzinger complex physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pre-Botzinger complex physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gustatory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gustatory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urinary bladder physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urinary bladder physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pituitary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pituitary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vascular endothelial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular endothelial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal uterine NK cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterine NK cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motile primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hypothalamus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hypothalamus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal splenocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal splenocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thyroid gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroid gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renal/urinary system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal/urinary system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal platelet dense granule physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal platelet dense granule physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eosinophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eosinophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bone marrow cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal autonomic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal autonomic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal chondrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chondrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal oligodendrocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oligodendrocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lysosome physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lysosome physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal enterocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enterocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymphatic system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymphatic system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal memory T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal memory T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal CD8-positive, alpha-beta T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal CD8-positive, alpha-beta T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal testis physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal marginal zone B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal marginal zone B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neural crest cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal surfactant physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal surfactant physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryonic tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryonic tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal carotid body physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal carotid body physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal granulocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal granulocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal NK T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal NK T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sebaceous gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sebaceous gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal peroxisome physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peroxisome physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hippocampus physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hippocampus physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal parotid gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parotid gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lung endothelial cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung endothelial cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal type I cell of carotid body physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal type I cell of carotid body physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal germinal center B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal germinal center B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sex gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sex gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal submandibular gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal regulatory T cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal regulatory T cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal oval cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oval cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Schwann cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Schwann cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal histamine physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal histamine physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vomeronasal sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vomeronasal sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gastroesophageal sphincter physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gastroesophageal sphincter physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T-helper 17 cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T-helper 17 cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal basophil physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal parasympathetic nervous system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parasympathetic nervous system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal GABAergic neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal GABAergic neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular endolymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular endolymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endolymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endolymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal follicular B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal follicular B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland myoepithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland myoepithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fibroblast physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fibroblast physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal synaptic physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synaptic physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endoplasmic reticulum physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endoplasmic reticulum physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal PP cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal PP cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal plasmacytoid dendritic cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal plasmacytoid dendritic cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Meibomian gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Meibomian gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sympathetic neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sympathetic neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal perilymph physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal perilymph physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic endocrine progenitor cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic endocrine progenitor cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placenta physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skin adnexa physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skin adnexa physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal T follicular helper cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal T follicular helper cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Paneth cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Paneth cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal memory B cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal memory B cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visceral endoderm physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visceral endoderm physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ureter physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ureter physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fetal cardiomyocyte physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ependyma motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ependyma motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pineal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pineal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intracellular organelle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intracellular organelle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestinal epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestinal epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestinal goblet cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestinal goblet cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal epididymis physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal epididymis physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sweat gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sweat gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuronal stem cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuronal stem cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic acinar cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic acinar cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal beige fat cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal beige fat cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart valve physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart valve physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visceral yolk sac physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visceral yolk sac physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal primary cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal primary cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neuroendocrine gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neuroendocrine gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cornea physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cornea physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mucous gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mucous gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal respiratory epithelium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cerebrospinal fluid physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebrospinal fluid physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal tear film physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tear film physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cartilage physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cartilage physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory sensory neuron physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory sensory neuron physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal non-rapid eye movement sleep pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye pigment epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye electrophysiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye electrophysiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye anterior chamber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye muscle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye anterior chamber depth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye movement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anterior eye segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior eye segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye blink conditioning behavior Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye blink conditioning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Involuntary Eye Movements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Involuntary Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Saccadic Eye Movement Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Saccadic Eye Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Rapid Eye Movement Sleep Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Rapid Eye Movement Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Conjugate Eye Movement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Conjugate Eye Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Eye Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Eye Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal eye development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal anterior eye segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye anterior chamber morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye distance/ position Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye distance/ position phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye electrophysiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye electrophysiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye blink conditioning behavior Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye blink conditioning behavior phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal non-rapid eye movement sleep pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior eye segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye movement Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye vasculature morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye posterior chamber depth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal eye anterior chamber depth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye anterior chamber depth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal eye morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
physiology Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term physiology in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
modification of morphology or physiology of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification of morphology or physiology of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification by host of symbiont morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification by host of symbiont morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by virus of host morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by virus of host morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification by symbiont of host morphology or physiology Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification by symbiont of host morphology or physiology biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of neutrophil physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of neutrophil physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of exocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of exocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiovascular system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of adrenal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of adrenal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of t cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of t cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of endocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of endocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skin physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skin physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skeletal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skeletal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of immune system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of immune system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the urinary system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Parathyroid Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Parathyroid Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Nervous System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Nervous System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Immune System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Immune System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Exocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Exocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Thyroid Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Thyroid Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of T Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of T Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Endocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Endocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of B Cell Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of B Cell Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Neutrophil Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Neutrophil Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Reproductive System Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Reproductive System Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality of immune system physiology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of immune system physiology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skin/hair/eye pigmentation, variation in, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fish-eye disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Eye Diseases, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Eye Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Eye Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases from the curated CTD Gene-Disease Associations dataset. |
Aland Island Eye Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Dry Eye Syndromes Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dry Eye Syndromes from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Eye Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Pain from the curated CTD Gene-Disease Associations dataset. |
Eye Infections, Bacterial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Infections, Bacterial from the curated CTD Gene-Disease Associations dataset. |
Eye Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Eye in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Eye Color Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Eye Color in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
eye disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
shipyard eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease shipyard eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dry eye syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dry eye syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aland island eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aland island eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye accommodation disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye accommodation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye and adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; retinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; sarcoidosis; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; sarcoidosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; hypersensitivity; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; macular degeneration; retinal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anophthalmos; coloboma; eye abnormalities; microphthalmos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anophthalmos; coloboma; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphakia; eye abnormalities; microphthalmos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphakia; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye movement disturbances Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye movement disturbances in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dry eye syndromes; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dry eye syndromes; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; corneal diseases; dry eye syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; corneal diseases; dry eye syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; pseudoxanthoma elasticum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; pseudoxanthoma elasticum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye abnormalities; glaucoma, angle-closure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye abnormalities; glaucoma, angle-closure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fish eye disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fish eye disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; eye diseases; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; eye diseases; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; stevens-johnson syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal ulcer; eye infections, bacterial; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal ulcer; eye infections, bacterial; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term eye in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eyelid development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eyelid development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye photoreceptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
compound eye corneal lens development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the compound eye corneal lens development biological process from the curated GO Biological Process Annotations 2015 dataset. |
cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of retina development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina vasculature morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina vasculature morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic cup formation involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
compound eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the compound eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens induction in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens induction in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
structural constituent of eye lens Gene SetFrom GO Molecular Function Annotations 2015 genes performing the structural constituent of eye lens molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Eye color traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Eye color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Eye color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
eye disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease eye disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
eye and adnexa disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease eye and adnexa disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia affecting the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slow saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the slow saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deeply set eye Gene SetFrom HPO Gene-Disease Associations genes associated with the deeply set eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eye of the tiger anomaly of globus pallidus Gene SetFrom HPO Gene-Disease Associations genes associated with the eye of the tiger anomaly of globus pallidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bull's eye maculopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the bull's eye maculopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hemorrhage of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the hemorrhage of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
uncontrolled eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the uncontrolled eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
poor hand-eye coordination Gene SetFrom HPO Gene-Disease Associations genes associated with the poor hand-eye coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior segment of eye aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hamartoma of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the hamartoma of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
paroxysmal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the paroxysmal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eye poking Gene SetFrom HPO Gene-Disease Associations genes associated with the eye poking phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vasculature of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
poor eye contact Gene SetFrom HPO Gene-Disease Associations genes associated with the poor eye contact phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent anterior eye chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the absent anterior eye chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Eye Hemorrhage Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Fungal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Fungal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Viral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Viral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Bacterial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Bacterial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cat eye syndrome critical region protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cat eye syndrome critical region protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cat eye syndrome critical region protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
hydropic eye lens fibers Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hydropic eye lens fibers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye opacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye opacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vision/eye phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged eye anterior chamber Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye bleb Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye bleb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
narrow eye opening Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the narrow eye opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[skin/hair/eye pigmentation 6, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 8] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, dark/light hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 10, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 6, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, black/nonblack hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, red hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 7, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
fish-eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the fish-eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset. |
microtia with nasolacrimal duct imperforation and eye coloboma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microtia with nasolacrimal duct imperforation and eye coloboma phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 4, fair/dark skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cat eye syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the cat eye syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/light eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
aland island eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the aland island eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
bornholm eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the bornholm eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
eye Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
eye cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
eye Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
anterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue anterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
vitreous chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue vitreous chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
compound eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue compound eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
eye cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue eye cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Eye-adipocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-adipocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-b cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-b cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-cd4-positive, alpha-beta t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-cd4-positive, alpha-beta t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-cd8-positive, alpha-beta t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-cd8-positive, alpha-beta t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-ciliary body Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-ciliary body relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-conjunctival epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-conjunctival epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-corneal epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-corneal epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-corneal keratocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-corneal keratocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-dendritic cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-dendritic cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-epithelial cell of lacrimal sac Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-epithelial cell of lacrimal sac relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-erythroid lineage cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-erythroid lineage cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-fibroblast Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-fibroblast relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-lacrimal gland functional unit cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-lacrimal gland functional unit cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-limbal stem cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-limbal stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-limbal stromal cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-limbal stromal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-macrophage Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-macrophage relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-mast cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-mast cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-melanocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-melanocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-microglial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-microglial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-monocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-monocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-muller cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-muller cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-ocular surface cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-ocular surface cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-plasma cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-plasma cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-radial glial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-radial glial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retina horizontal cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retina horizontal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal bipolar neuron Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal bipolar neuron relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal blood vessel endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal blood vessel endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal ganglion cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal ganglion cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal pigment epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal pigment epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Dry Eye Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dry Eye Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inflammatory Abnormality Of The Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Abnormality Of The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pterygium Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pterygium Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cat Eye Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cat Eye Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rieger Eye Malformation Sequence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rieger Eye Malformation Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye Disorder Due To Diabetes Mellitus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eye Disorder Due To Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bornholm Eye Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bornholm Eye Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Eye Brain Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscle Eye Brain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fish-Eye Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fish-Eye Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Anomaly Of Anterior Segment Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomaly Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Malformations Of Anterior Segment Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Infection Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Eye Disorders (Excl Glaucoma) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Eye Disorders (Excl Glaucoma) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Rapid Eye Movement Parasomnia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Rapid Eye Movement Parasomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye Poking Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eye Poking in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dermoid Choristoma Of Eye Proper Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dermoid Choristoma Of Eye Proper in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bull'S Eye Macular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bull'S Eye Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dryness Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dryness Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Paroxysmal Involuntary Eye Movements Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paroxysmal Involuntary Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Depth Of Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Depth Of Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Coloboma (In Some Patients) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Coloboma (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Poor Eye Contact Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Eye Contact in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shallow Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shallow Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Color Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Color in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Injected Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Injected Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Manifestations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Manifestations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Uncontrolled Eye Movements Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uncontrolled Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Redness Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Redness Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deep Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deep Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Of The Tiger Anomaly Of Globus Pallidus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Of The Tiger Anomaly Of Globus Pallidus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Affecting The Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Affecting The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Segment Of Eye Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Segment Of Eye Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Problem Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Problem in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Poor Hand-Eye Coordination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Hand-Eye Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Around Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Around Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
vertebrate eye-specific patterning Gene SetFrom GO Biological Process Annotations 2023 genes participating in the vertebrate eye-specific patterning biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
lens placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lens placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset. |
avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset. |
absent eye anterior chamber Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye anterior chamber phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
narrow eye opening Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the narrow eye opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hydropic eye lens fibers Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hydropic eye lens fibers phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye opacity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye opacity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye bleb Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye bleb phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged eye anterior chamber Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye lesions Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
variegated eye pigmentation pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the variegated eye pigmentation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye discharge Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye discharge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vision/eye phenotype Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
narrow eye opening Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the narrow eye opening phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
eye hemorrhage Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the eye hemorrhage phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Fetal Development - L2 - Eye-Ganglion cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Stromal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Vascular endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Astrocytes Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Microglia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Photoreceptor cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Skeletal muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Smooth muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Horizontal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Amacrine cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Bipolar cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Bipolar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Lens fibre cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
vertebrate eye-specific patterning Gene SetFrom GO Biological Process Annotations 2025 genes participating in the vertebrate eye-specific patterning biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
lens placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lens placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset. |
avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Eye disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Eye disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Eye degenerative disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Eye disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Eye disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Eye degenerative disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dry eye syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dry eye syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aland Island eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aland Island eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye accommodation disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye accommodation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Shipyard eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Shipyard eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lateral displacement of eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lateral displacement of eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with eye movement abnormalities and ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with eye movement abnormalities and ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Blind hypotensive eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blind hypotensive eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Compound eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Compound eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Vitreous chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vitreous chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Anterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Eye cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
SKIN/HAIR/EYE PIGMENTATION Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTATION phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormality of the eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of the eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormality of eye movement Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of eye movement phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Deeply set eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Deeply set eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fish-eye disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SKIN/HAIR/EYE PIGMENTAT Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTAT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aland island eye disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aland island eye disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PITX2-Related Eye Abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PITX2-Related Eye Abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Disorder of eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Disorder of eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced eye contact Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced eye contact phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (brightness) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (brightness) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (saturation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (saturation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (hue) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (hue) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Skin, hair and eye pigmentation (multivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Skin, hair and eye pigmentation (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye morphology Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye length Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye movement (horizontal position gain) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye movement (horizontal position gain) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye movement in schizophrenia (horizontal position gain) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye movement in schizophrenia (horizontal position gain) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |