All diseases

OMIM ID
219150
OMIM term:
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA; ARCL3A
Alternative terms:
DE BARSY SYNDROME A
CUTIS LAXA, CORNEAL CLOUDING, AND MENTAL RETARDATION
PROGEROID SYNDROME OF DE BARSY
(∗) Location:
10q24.1  
(†) Associated OMIM genes:
ALDH18A1  
(‡) Associated MGI genes:

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