Hemophilia A
Disease ID: disease_node_3828
Connections displayed (default: 10).
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| Dbxref | GARD:6591, ICD10CM:D66, ICD9CM:286.0, MESH:D006467, MIM:306700, NCI:C27146, ORDO:98878, SNOMEDCT_US_2023_03_01:28293008, UMLS_CUI:C0019069 |
|---|---|
| Subclassof | DOID_0080012, DOID_0061030 |
| Data Source | DOID, MESH |
| Synonyms | Congenital factor VIII disorder, Hemophilia A, Subhemophilia, classic hemophilia, classic hemophilia A |
| Mesh Id | D006467 |
| Mesh Label | Hemophilia A |
| Mesh Subclassof | D020147, D025861, D006474 |
| Doid Label | factor VIII deficiency |
| Doid Description | A hemophilia that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_3828 |
| Doid Id | DOID_12134 |
| Label | Hemophilia A |
- Outgoing r'ship
SUBCLASS_OFto/from Hemophilia(ID:disease_node_15603) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)