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Human Disease and Mouse Model Detail
Human Disease Lipodystrophy, Familial Partial, Type 3; FPLD3
OMIM ID: 604367
Synonyms Lipodystrophy, Familial Partial; Lipodystrophy, Familial Partial, Associated with PPARG Mutations
View all models View ALL (3) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PPARG* Pparg* View 3 models HomoloGene
     PPP1R3A* Ppp1r3a   HomoloGene and HGNC
References Disease References using Mouse Models (2)

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 6.03
The Jackson Laboratory