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DO Term : familial partial lipodystrophy type 3 [DOID:0070204] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.

synonyms:
FPLD3,
PPARG-related familial partial lipodystrophy,
604367,
GARD:12600,
UMLS_CUI:C1720861,
SNOMEDCT_US_2023_03_01:1197745002,
OMIM:604367,
PPARG-related FPLD,
familial partial lipodystrophy associated with PPARG mutations,
MESH:D052496,
ORDO:79083

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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