Factor Vii Deficiency
Disease ID: disease_node_3140
Connections displayed (default: 10).
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| Dbxref | GARD:2238, ICD10CM:D68.2, MESH:D005168, MIM:227500, NCI:C131631, ORDO:327, SNOMEDCT_US_2023_03_01:154820003, UMLS_CUI:C0015503 |
|---|---|
| Subclassof | DOID_0050737, DOID_1247 |
| Data Source | DOID, MESH |
| Synonyms | deficiency, stable |
| Mesh Id | D005168 |
| Mesh Label | Factor VII Deficiency |
| Disease Has Feature | DOID_801 |
| Mesh Subclassof | D020147, D025861, D006474 |
| Doid Label | factor VII deficiency |
| Doid Description | A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. |
| Has Symptom | SYMP_0000756, SYMP_0000742, SYMP_0000007, SYMP_0000448 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_3140 |
| Doid Id | DOID_2215 |
| Label | Factor Vii Deficiency |
- Outgoing r'ship
HAS_SYMPTOMto/from Menorrhagia(ID:disease_node_5150;disease_node_21571) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Gum Bleeding(ID:disease_node_21673) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Epistaxis(ID:disease_node_2998;disease_node_21658) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Bleeding(ID:disease_node_21108) (Disease) - 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)