Factor X Deficiency
Disease ID: disease_node_3144
Connections displayed (default: 10).
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| Dbxref | GARD:6404, MESH:D005171, MIM:227600, NCI:C131632, ORDO:328, SNOMEDCT_US_2023_03_01:76642003, UMLS_CUI:C0015519 |
|---|---|
| Subclassof | DOID_0050737, DOID_1247 |
| Data Source | DOID, MESH |
| Synonyms | disease, Stuart-Prower |
| Mesh Id | D005171 |
| Mesh Label | Factor X Deficiency |
| Mesh Subclassof | D020147, D025861, D006474 |
| Doid Label | factor X deficiency |
| Doid Description | A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_3144 |
| Doid Id | DOID_2222 |
| Label | Factor X Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Blood Coagulation Disorders(ID:disease_node_1621) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)