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Human Disease and Mouse Model Detail
Human Disease Lipodystrophy, Partial, Acquired, with Low Complement Component C3, with or without Glomerulonephritis; APLDC3
OMIM ID: 613913
Human Phenotype Ontology associations
Synonyms Lipodystrophy, Partial, Acquired, Associated with C3 Nephritic Factor
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory