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OBO ID: DOID:0070204
Term Name: familial partial lipodystrophy type 3 Search Ontology:
Synonyms:
  • familial partial lipodystrophy associated with PPARG mutations
  • FPLD3
  • PPARG-related familial partial lipodystrophy
  • PPARG-related FPLD
Definition: A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25. https://www.ncbi.nlm.nih.gov/pubmed/10622252
References:
Ontology: Human Disease   (DOID:0070204)
OTHER familial partial lipodystrophy type 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PPARG Lipodystrophy, familial partial, type 3 604367
Insulin resistance, severe, digenic 604367
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None