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Cutis laxa, autosomal dominant 1

MONDO:0007411

Any autosomal dominant cutis laxa in which the cause of the disease is a mutation in the ELN gene.

Also known as: cutis laxa, autosomal dominant, ADCL1, ELN autosomal dominant cutis laxa, autosomal dominant cutis laxa caused by mutation in ELN, cutis laxa, autosomal dominant 1, cutis laxa, autosomal dominant type 1, autosomal dominant cutis laxa 1

0 clinical trials for this condition and its sub-types, 0 tagged with Cutis laxa, autosomal dominant 1 itself.

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