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Birt-Hogg-Dube syndrome 2

MONDO:0800455

Birt-Hogg-Dube syndrome caused by the mutations in PRDM10.

Also known as: BHD2

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Human disease (14) Birt-Hogg-Dube syndrome (2) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0) Disease by etiologic mechanism (0)

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