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Fascial dystrophy, congenital

MONDO:0009219

Also known as: fascial dystrophy, congenital

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

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Stiff skin syndrome (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Integumentary system disorder (0)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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