- OMIM ID
-
219200
- OMIM term:
- CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A
- Alternative terms:
-
ARCL2
CUTIS LAXA WITH CONGENITAL DISORDER OF GLYCOSYLATION
CUTIS LAXA WITH GROWTH AND DEVELOPMENTAL DELAY
CUTIS LAXA, DEBRE TYPE
CUTIS LAXA WITH BONE DYSTROPHY
CUTIS LAXA WITH JOINT LAXITY AND RETARDED DEVELOPMENT
- (∗) Location:
- 12q24.31
- (†) Associated OMIM genes:
- ATP6V0A2
- (‡) Associated MGI genes:
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