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

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Broader categories

Disease (680) Hereditary disease (176) Cutis laxa (37) Human disease (14) Developmental defect during embryogenesis (8) Disease of genetic or genomic mechanism (2) Autosomal dominant cutis laxa (0) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0)

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