Oculocutaneous Albinism Type Vii
Disease ID: disease_node_19187
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| Dbxref | MIM:615179 |
|---|---|
| Subclassof | DOID_0050632 |
| Data Source | DOID |
| Synonyms | OCA7 |
| Doid Label | oculocutaneous albinism type VII |
| Doid Description | An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3. |
| Disease Node Id | disease_node_19187 |
| Doid Id | DOID_0070100 |
| Label | Oculocutaneous Albinism Type Vii |
- Outgoing r'ship
SUBCLASS_OFto/from Albinism, Oculocutaneous(ID:disease_node_8609) (Disease)