Platelet-Type Bleeding Disorder 9
Disease ID: disease_node_17053
Connections displayed (default: 10).
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| Dbxref | ICD10CM:D69.8, MIM:614200, ORDO:98886 |
|---|---|
| Subclassof | DOID_0050736, DOID_2218 |
| Data Source | DOID |
| Synonyms | BDPLT9, GP Ia deficiency, collagen platelet receptor deficiency, glycoprotein Ia deficiency |
| Doid Label | platelet-type bleeding disorder 9 |
| Doid Description | A blood platelet disease characterized by autosomal domit inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has_material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17053 |
| Doid Id | DOID_0111045 |
| Label | Platelet-Type Bleeding Disorder 9 |
- Outgoing r'ship
SUBCLASS_OFto/from Blood Platelet Disorders(ID:disease_node_1622) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)