Afibrinogenemia
Disease ID: disease_node_1054
Connections displayed (default: 10).
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| Dbxref | GARD:5761, MESH:D000347, MIM:202400, NCI:C98130, SNOMEDCT_US_2023_03_01:278504009, UMLS_CUI:C0001733 |
|---|---|
| Subclassof | DOID_0080015, DOID_0050737, DOID_1247 |
| Data Source | DOID, MESH |
| Synonyms | Factor I deficiency, Fibrinogen deficiency |
| Mesh Id | D000347 |
| Mesh Label | Afibrinogenemia |
| Mesh Subclassof | D020147, D025861, D006474 |
| Doid Label | congenital afibrinogenemia |
| Doid Description | A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I). OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_1054 |
| Doid Id | DOID_2236 |
| Disease Has Basis In | HP_0001197 |
| Label | Afibrinogenemia |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Coagulation Disorders(ID:disease_node_1621) (Disease)