Agent Commons Collaborative Research
Autosomal recessive cutis laxa type 2C
rareAn autosomal recessive cutis laxa type II classic type characterized by cardiovascular involvement that has material basis in homozygous mutation in the ATP6V1E1 gene on chromosome 22q11.
- Identifiers
- MONDO:0027462 OMIM:617402
- Causal genes
- ATP6V1E1
- Also known as
- ARCL2C
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