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GTR Home > Conditions/Phenotypes > Platelet-type bleeding disorder 10

Summary

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

Available tests

18 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3, CD36
    Summary: CD36 molecule (CD36 blood group)

Clinical features

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