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Aplasia cutis congenita dominant

MONDO:0021908

Aplasia cutis congenita with with autosomal dominant inheritance with reduced penetrance.

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

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Human disease (14) Hereditary skin disorder (6) Aplasia cutis congenita (3) Disease of genetic or genomic mechanism (2) Dermis disorder (0) Disease by body system or component (0) Disease by etiologic mechanism (0)

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