Protein C Deficiency
Disease ID: disease_node_10116
Connections displayed (default: 10).
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| Dbxref | GARD:4521, ICD10CM:D68.59, MESH:D020151, NCI:C99025, ORDO:745, SNOMEDCT_US_2023_03_01:76407009, UMLS_CUI:C0398625 |
|---|---|
| Subclassof | DOID_0050736, DOID_2452 |
| Data Source | DOID, MESH |
| Mesh Id | D020151 |
| Mesh Label | Protein C Deficiency |
| Mesh Subclassof | D025861, D001796, D019851 |
| Doid Label | protein C deficiency |
| Doid Description | A thrombophilia that is characterized by recurrent venous thrombosis and that has_material_basis_in heterozygous mutation in the PROC gene on chromosome 2q14. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_10116 |
| Doid Id | DOID_3756 |
| Label | Protein C Deficiency |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Thrombophilia(ID:disease_node_10025) (Disease)