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| Term | platelet-type bleeding disorder 11 | ID (Ontology) | DOID:0111057 (Human Disease) |
| Definition | A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13. | ||
| Also Known As | "BDPLT11" ; "glycoprotein VI deficiency" ; "GP VI deficiency" | ||
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autosomal genetic disease |__autosomal recessive disease__ blood coagulation disease | |__blood platelet disease_______| platelet-type bleeding disorder 11 |
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| Is a |
autosomal recessive disease blood platelet disease |
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ICD10CM:D69.8 MIM:614201 ORDO:98885 |
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