PPARG-related familial partial lipodystrophy
Also known as FPLD3, PPARG-related FPLD, familial partial lipodystrophy type 3, familial partial lipodystrophy associated with PPARG mutations+3 more
FPLD3, PPARG-related FPLD, familial partial lipodystrophy type 3, familial partial lipodystrophy associated with PPARG mutations, insulin resistance, severe, digenic, lipodystrophy, familial partial, associated with Pparg mutations, lipodystrophy, familial partial, type 3.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
FPLD3, PPARG-related FPLD, familial partial lipodystrophy type 3, familial partial lipodystrophy associated with PPARG mutations, insulin resistance, severe, digenic, lipodystrophy, familial partial, associated with Pparg mutations, lipodystrophy, familial partial, type 3
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.