All diseases

OMIM ID
613327
OMIM term:
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4
Alternative terms:
BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 4, WITH MUSCULAR DYSTROPHY
LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 4, WITH MUSCULAR DYSTROPHY
(∗) Location:
17q21.2  
(†) Associated OMIM genes:
PTRF  
(‡) Associated MGI genes:
Ptrf  

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