Albinism, Oculocutaneous
Disease ID: disease_node_8609
Connections displayed (default: 10).
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| Dbxref | GARD:10958, ICD10CM:E70.3, MESH:D016115, MIM:PS203100, ORDO:55 |
|---|---|
| Subclassof | DOID_225, DOID_0050737 |
| Data Source | DOID, MESH |
| Mesh Id | D016115 |
| Mesh Label | Albinism, Oculocutaneous |
| Mesh Subclassof | D000417 |
| Doid Label | oculocutaneous albinism |
| Doid Description | A syndrome characterized by abnormal pigmentation of the skin, hair and eyes. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_8609 |
| Doid Id | DOID_0050632 |
| Label | Albinism, Oculocutaneous |
- Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type Iii(ID:disease_node_19190) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type Vii(ID:disease_node_19187) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type Ia(ID:disease_node_19191) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type Vi(ID:disease_node_19186) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type Iv(ID:disease_node_19189) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculocutaneous Albinism Type V(ID:disease_node_19188) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)