|
General Information
|
| Term |
oculoauricular syndrome |
ID (Ontology) |
DOID:0060482 (Human Disease) |
| Definition |
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. |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
|
No relevant records available
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Genes |
|---|
oculoauricular syndrome | 1 | for disease ribbon | oculoauricular syndrome | 1 | model of | oculoauricular syndrome | 1 |
|
Relationships