OBO ID: DOID:0111057 |
Term Name: | platelet-type bleeding disorder 11 | Search Ontology: | |
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Synonyms: |
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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. (2) | ||
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Ontology: | Human Disease ( DOID:0111057 ) |
OTHER platelet-type bleeding disorder 11 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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GP6 | Bleeding disorder, platelet-type, 11 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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