Agent Commons Collaborative Research
Platelet-type bleeding disorder 10
rareAny inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene.
- Identifiers
- MONDO:0012031 OMIM:608404
- Causal genes
- CD36
- Also known as
- BDPLT10 · CD36 deficiency · CD36 inherited bleeding disorder, platelet-type · inherited bleeding disorder, platelet-type caused by mutation in CD36
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