inherited bleeding disorder, platelet-type
MONDO:0000009Mondo
Findings
No curated finding names inherited bleeding disorder, platelet-type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- Narrower terms (35)
- Bernard-Soulier syndrome
- bleeding diathesis due to thromboxane synthesis deficiency
- bleeding disorder, platelet-type, 21
- bleeding disorder, platelet-type, 22
- bleeding disorder, platelet-type, 24
- bleeding disorder, platelet-type, 25
- congenital thrombotic thrombocytopenic purpura
- cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
- Ehlers-Danlos syndrome, fibronectinemic type
- Glanzmann thrombasthenia
- gray platelet syndrome
- macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
- P2RY12-related platelet disorder, autosomal dominant
- platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
- platelet-type bleeding disorder 10
Other names
1 name
Resolves to: inherited bleeding disorder, platelet-type
- Also called
- bleeding disorder, platelet-type