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Autosomal recessive cutis laxa type 2D
rareAn autosomal recessive cutis laxa type II classic type characterized by cardiovascular and neurologic involvement and that has material basis in homozygous mutation in the ATP6V1A gene on chromosome 3q13.
- Identifiers
- MONDO:0027451 OMIM:617403
- Causal genes
- ATP6V1A
- Also known as
- ARCL2D
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