optic nerve dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of developmental dysplasia of the optic nerve. (Human Phenotype Ontology, HP_0001093)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001093
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Genes

5 genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD3 ATP-binding cassette, sub-family D (ALD), member 3
BRAF B-Raf proto-oncogene, serine/threonine kinase
MITF microphthalmia-associated transcription factor
PEX5 peroxisomal biogenesis factor 5
TYR tyrosinase