Oculocutaneous Albinism Type V
Disease ID: disease_node_19188
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:615312 |
|---|---|
| Subclassof | DOID_0050632 |
| Data Source | DOID |
| Synonyms | OCA5 |
| Doid Label | oculocutaneous albinism type V |
| Doid Description | An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA5 gene on chromosome 4q24. |
| Disease Node Id | disease_node_19188 |
| Doid Id | DOID_0070099 |
| Label | Oculocutaneous Albinism Type V |
- Outgoing r'ship
SUBCLASS_OFto/from Albinism, Oculocutaneous(ID:disease_node_8609) (Disease)