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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
PPARG-related familial partial lipodystrophy
FPLD3 · Familial partial lipodystrophy type 3
AKT2-related familial partial lipodystrophy
AKT2-related FPLD
CIDEC-related familial partial lipodystrophy
FPLD5 · CIDEC-related FPLD
LIPE-related familial partial lipodystrophy
FPLD6 · LIPE-related FPLD
PLIN1-related familial partial lipodystrophy
FPLD4 · PLIN1-related FPLD