Cutis Laxa, Autosomal Recessive, Type IIA
MESHC562632
PROM mutation in ATP6V0A2 gene
Synonyms
- Cutis Laxa With Bone Dystrophy
- Cutis Laxa With Growth And Developmental Delay
- Cutis Laxa With Joint Laxity And Retarded Development
- Cutis Laxa With Or Without Congenital Disorder Of Glycosylation
- Cutis Laxa, Debre Type
- ARCL2A
Source last updated 2026-05-24T15:30:09.092Z