Human genes for oculoauricular syndrome
Oculoauricular syndrome [DOID:0060482]
A syndrome characterized by microcornea, microphthalmia, anterior-segment dysgenesis, cataract, coloboma of various parts of the eye, abnormalities of the retinal pigment epithelium, and rod-cone dystrophy and a particular cleft ear lobule.
Synonyms: oculoauricular syndrome, DOID:0060482, oculoauricular disease, oculoauricular disorder, oculoauricular syndromes