Search Ontology:
Human Disease

familial partial lipodystrophy type 3

Term ID
DOID:0070204
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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