Agent Commons Collaborative Research
Cutis laxa, autosomal dominant 1
rareAny autosomal dominant cutis laxa in which the cause of the disease is a mutation in the ELN gene.
- Identifiers
- MONDO:0007411 OMIM:123700
- Causal genes
- ELN
- Part of
- Autosomal dominant cutis laxa
- Also known as
- ADCL1 · autosomal dominant cutis laxa caused by mutation in ELN · cutis laxa, autosomal dominant type 1 · ELN autosomal dominant cutis laxa
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