Cutis laxa, autosomal dominant 2

MONDO:0013751

Any autosomal dominant cutis laxa in which the cause of the disease is a mutation in the FBLN5 gene.

Also known as: FBLN5 autosomal dominant cutis laxa, autosomal dominant cutis laxa caused by mutation in FBLN5, cutis laxa, autosomal dominant 2, cutis laxa, autosomal dominant type 2, ADCL2

0 clinical trials for this condition and its sub-types, 0 tagged with Cutis laxa, autosomal dominant 2 itself.

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↑ Autosomal dominant cutis laxa (0)

Including sub-types (0) Tagged with Cutis laxa, autosomal dominant 2 (0)

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