| Human Disease |
Term: Lipodystrophy, Congenital Generalized, Type 3; CGL3
OMIM ID: 612526
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| Synonyms |
Berardinelli-Seip Congenital Lipodystrophy, Type 3; BSCL3; Lipodystrophy, Berardinelli-Seip Congenital, Type 3 |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
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Analysis Tools