| Human Disease |
Lipodystrophy, Congenital Generalized, Type 3; CGL3 OMIM ID: 612526 |
|||||||||||||||||||||
| Synonyms | Berardinelli-Seip Congenital Lipodystrophy, Type 3; BSCL3; Lipodystrophy, Berardinelli-Seip Congenital, Type 3 | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
|
|
|
||