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DOID:0060841 - isolated microphthalmia 8
Disease Ontology Definition:A microphthalmia characterized by bilateral severe microphthalmia autosomal recessive inheritance of that has_material_basis_in homozygous mutation in the ALDH1A3 gene on chromosome 15q26.
Synonyms: MCOP8,
Echinobase Genes :
MIM:615113 - microphthalmia, isolated 8; mcop8 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
microphthalmia (is_a)