platelet-type bleeding disorder 10
MONDO:0012031Mondo
Findings
No curated finding names platelet-type bleeding disorder 10 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene.
Definition from the Mondo Disease Ontology (MONDO:0012031), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Genes
1 gene
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.
- CD36HGNC:1663
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · Laboratory for Molecular Medicine · Autosomal recessive · 2020
Where it sits
Other names
4 names
Resolves to: platelet-type bleeding disorder 10
- Also called
- BDPLT10CD36 deficiencyCD36 inherited bleeding disorder, platelet-typeinherited bleeding disorder, platelet-type caused by mutation in CD36