familial partial lipodystrophy type 3

Summary
Synonym
  • FPLD3
  • PPARG-related FPLD
  • PPARG-related familial partial lipodystrophy
  • familial partial lipodystrophy associated with PPARG mutations
Definition
A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.
Super Class
autosomal dominant disease familial partial lipodystrophy
Disease Ontology
DOID:0070204
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5468 PPARG peroxisome proliferator activated receptor gamma
Displaying 1 entry
Gene ID Gene Symbol Description Source
19016 Pparg peroxisome proliferator activated receptor gamma
Displaying 1 entry
Gene ID Gene Symbol Description Source
25664 Pparg peroxisome proliferator-activated receptor gamma

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024