Platelet-Type Bleeding Disorder 10
Disease ID: disease_node_17064
Connections displayed (default: 10).
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| Dbxref | MIM:608404 |
|---|---|
| Subclassof | DOID_0050737, DOID_2218 |
| Data Source | DOID |
| Synonyms | BDPLT10, CD36 deficiency, platelet glycoprotein IV deficiency |
| Doid Label | platelet-type bleeding disorder 10 |
| Doid Description | A blood platelet disease characterized by autosomal recessive inheritance of variable bleeding tendency, thrombocytopenia, giant platelets, and prolonged bleeding times that has_material_basis_in homozygous or compound heterozygous mutation in the CD36 antigen gene on chromosome 7q21. |
| Has Symptom | SYMP_0000007 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17064 |
| Doid Id | DOID_0111046 |
| Label | Platelet-Type Bleeding Disorder 10 |
- Outgoing r'ship
HAS_SYMPTOMto/from Bleeding(ID:disease_node_21108) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Blood Platelet Disorders(ID:disease_node_1622) (Disease)