Griscelli Syndrome
Disease ID: disease_node_18455
Connections displayed (default: 10).
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| Dbxref | GARD:10913, ICD10CM:E70.3, MIM:PS214450, ORDO:381 |
|---|---|
| Subclassof | DOID_16, DOID_0050737 |
| Data Source | DOID |
| Synonyms | Chediak-Higashi-like syndrome, Griscelli-Prunieras syndrome, partial albinism-immunodeficiency syndrome |
| Doid Label | Griscelli syndrome |
| Doid Description | An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18455 |
| Doid Id | DOID_0060831 |
| Label | Griscelli Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Integumentary System Disease(ID:disease_node_13866) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)