Details of Disease | DrugMAP

General Information of Disease (ID: DISNNCXT)

Disease Name	Platelet-type bleeding disorder 10
Synonyms	bleeding disorder, Platelet-type, 10; platelet glycoprotein 4 deficiency; inherited bleeding disorder, platelet-type caused by mutation in CD36; BDPLT10; platelet glycoprotein IV deficiency; platelet-type bleeding disorder 10; CD36 deficiency; CD36 inherited bleeding disorder, platelet-type
Definition	Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene.
Disease Hierarchy	DIS1DL2M: Inherited blood coagulation disorder DISIUNXT: Inherited bleeding disorder, platelet-type DISNNCXT: Platelet-type bleeding disorder 10
Disease Identifiers	MONDO ID MONDO_0012031 MESH ID C564245 UMLS CUI C1842090 OMIM ID 608404 MedGen ID 374856

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
CD36	TTPJMCU	Strong	Autosomal recessive	[1]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CNN1	OTVPG39Z	Limited	Altered Expression	[2]
CD36	OT5CZWKY	Strong	Autosomal recessive	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.
2	CD36 Enhances Vascular Smooth Muscle Cell Proliferation and Development of Neointimal Hyperplasia.Arterioscler Thromb Vasc Biol. 2019 Feb;39(2):263-275. doi: 10.1161/ATVBAHA.118.312186.