Platelet-type bleeding disorder 10

Definition

Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene.

Also known as BDPLT10, CD36 deficiency, CD36 inherited bleeding disorder, platelet-type, inherited bleeding disorder, platelet-type caused by mutation in CD36, platelet-type bleeding disorder 10 — per MONDO

Also identified as

• DOID 0111046 per MONDO
• MESH C564245 per MONDO
• OMIM 608404 per MONDO
• UMLS C1842090 per MONDO