Factor V Deficiency
Disease ID: disease_node_3136
Connections displayed (default: 10).
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| Dbxref | GARD:2237, ICD10CM:D68.2, MESH:D005166, MIM:227400, NCI:C98938, SNOMEDCT_US_2023_03_01:191284007, UMLS_CUI:C0015499 |
|---|---|
| Subclassof | DOID_0050737, DOID_1247 |
| Data Source | DOID, MESH |
| Synonyms | Hereditary hypoproaccelerinaemia, Labile factor deficiency, Proaccelerin deficiency, deficiency, labile |
| Mesh Id | D005166 |
| Mesh Label | Factor V Deficiency |
| Mesh Subclassof | D020147, D025861, D006474 |
| Doid Label | factor V deficiency |
| Doid Description | OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_3136 |
| Doid Id | DOID_2216 |
| Label | Factor V Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Coagulation Disorders(ID:disease_node_1621) (Disease)