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Epidermolysis bullosa simplex with anodontia/hypodontia

MONDO:0016514

Also known as: Gamborg-Nielsen syndrome, Kallin syndrome

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

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Epidermolysis bullosa (21) Human disease (14) Hereditary skin disorder (5) Inherited epidermolysis bullosa (5) Epidermolysis bullosa simplex (4) Vesiculobullous skin disease (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2
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