oculoauricular syndrome
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
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oculoauricular syndrome
Summary
oculoauricular syndrome is a developmental defect during embryogenesis[1]. It draws 118 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- oculoauricular syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- oculoauricular syndrome's instance of is recorded as rare disease[4].
- oculoauricular syndrome's instance of is recorded as class of disease[5].
- oculoauricular syndrome is a type of syndrome[6].
- oculoauricular syndrome is a type of syndromic microphthalmia[7].
- oculoauricular syndrome's health specialty is recorded as medical genetics[8].
- oculoauricular syndrome's genetic association is recorded as HMX1[9].
- oculoauricular syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060482[10].
- oculoauricular syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060482[11].
- oculoauricular syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_157962[12].
- oculoauricular syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
oculoauricular syndrome draws 118 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] It is known by 7 alternative names across languages and contexts.[14]