/cutis laxa, autosomal dominant 2

cutis laxa, autosomal dominant 2

Rare Disease

MONDO:0013751

Also Known As

FBLN5 autosomal dominant cutis laxaautosomal dominant cutis laxa 2autosomal dominant cutis laxa caused by mutation in FBLN5cutis laxa, autosomal dominant 2cutis laxa, autosomal dominant type 2ADCL2

Definition

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

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Associated Genes

FBLN5 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614434 ↗

GARD

GARD:15802 ↗

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