Wiskott-Aldrich Syndrome
Disease ID: disease_node_7992
Connections displayed (default: 10).
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| Dbxref | ICD10CM:D82.0, ICD9CM:279.12, MESH:D014923, MIM:301000, NCI:C3448, SNOMEDCT_US_2023_03_01:36070007, UMLS_CUI:C0043194 |
|---|---|
| Subclassof | DOID_0080012, DOID_225 |
| Data Source | DOID, MESH |
| Synonyms | Wiskott syndrome |
| Mesh Id | D014923 |
| Mesh Label | Wiskott-Aldrich Syndrome |
| Mesh Subclassof | D025861, D006474, D000081207, D008231, D040181 |
| Doid Label | Wiskott-Aldrich syndrome |
| Doid Description | A syndrome that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia). OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_7992 |
| Doid Id | DOID_9169 |
| Label | Wiskott-Aldrich Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)