All diseases

OMIM ID
608594
OMIM term:
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1; CGL1
Alternative terms:
BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 1; BSCL1
LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 1
BRUNZELL SYNDROME, AGPAT2-RELATED
(∗) Location:
9q34.3  
(†) Associated OMIM genes:
AGPAT2  
(‡) Associated MGI genes:
Agpat2  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/mwn90cm8