Platelet-Type Bleeding Disorder 12
Disease ID: disease_node_17054
Connections displayed (default: 10).
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| Dbxref | MIM:605735 |
|---|---|
| Subclassof | DOID_0050736, DOID_2218 |
| Data Source | DOID |
| Synonyms | BDPLT12, PGHS1 deficiency, platelet COX1 deficiency, platelet cyclooxygenase 1 deficiency, platelet prostaglandin-endoperoxide synthase 1 deficiency |
| Doid Label | platelet-type bleeding disorder 12 |
| Doid Description | A blood platelet disease characterized by autosomal domit inheritance of mildly increased bleeding, platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity. |
| Has Symptom | SYMP_0000007 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17054 |
| Doid Id | DOID_0111058 |
| Label | Platelet-Type Bleeding Disorder 12 |
- Outgoing r'ship
HAS_SYMPTOMto/from Bleeding(ID:disease_node_21108) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Platelet Disorders(ID:disease_node_1622) (Disease)