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Metadata
ID DOID:0111057
Name platelet-type bleeding disorder 11
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.
https://www.ncbi.nlm.nih.gov/pubmed/19549989, https://www.ncbi.nlm.nih.gov/pubmed/19552682
Xrefs

ICD10CM:D69.8

MIM:614201

ORDO:98885

Subsets

DO_rare_slim

Synonyms

BDPLT11 [EXACT]

glycoprotein VI deficiency [EXACT]

GP VI deficiency [EXACT]

Parent Relationships

is_a blood platelet disease

is_a autosomal recessive disease

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