All diseases

OMIM ID
269700
OMIM term:
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2; CGL2
Alternative terms:
BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 2
SEIP SYNDROME
BERARDINELLI SYNDROME
LIPODYSTROPHY, TOTAL, AND ACROMEGALOID GIGANTISM
LIPOATROPHIC DIABETES, CONGENITAL
LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 2
BRUNZELL SYNDROME, BSCL2-RELATED
(∗) Location:
11q12.3  
(†) Associated OMIM genes:
BSCL2  
(‡) Associated MGI genes:
Bscl2   Pparg  

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