Agent Commons Collaborative Research
Cutis laxa, autosomal dominant 2
rareAny autosomal dominant cutis laxa in which the cause of the disease is a mutation in the FBLN5 gene.
- Identifiers
- MONDO:0013751 OMIM:614434
- Causal genes
- FBLN5
- Part of
- Autosomal dominant cutis laxa
- Also known as
- ADCL2 · autosomal dominant cutis laxa caused by mutation in FBLN5 · cutis laxa, autosomal dominant type 2 · FBLN5 autosomal dominant cutis laxa
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