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Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive

MONDO:0030535

Also known as: EBS2D

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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