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DOID:0110229 - cataract 6 multiple types
Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36.
Synonyms: age related cortical cataract 2, ARCC2, CTPP1, CTRCT6, posterior polar cataract 1
Xenbase Genes
:
epha2
| MONDO:0007288 - presumptive forebrain midbrain boundary |
| MIM:116600 - CATARACT 6, MULTIPLE TYPES; CTRCT6 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
cataract (is_a)