FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial partial lipodystrophy type 6 ID (Ontology) DOID:0070206 (Human Disease)
Definition A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the LIPE gene on chromosome 19q13.
Also Known As "familial partial lipodystrophy associated with LIPE mutations" ; "FPLD6" ; "LIPE-related familial partial lipodystrophy" (for all, see Synonyms field below)
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 Genes
 familial partial lipodystrophy type 6       1
 for disease ribbon | familial partial lipodystrophy type 6       1
 model of | familial partial lipodystrophy type 6       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease_____
partial lipodystrophy               |
 |__familial partial lipodystrophy__|
                                    familial partial lipodystrophy type 6  1 rec.
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Is a familial partial lipodystrophy
autosomal recessive disease
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Synonyms
  • "familial partial lipodystrophy associated with LIPE mutations" EXACT
    "FPLD6" EXACT OMO:0003012
    "LIPE-related familial partial lipodystrophy" EXACT
    "LIPE-related FPLD" EXACT
Secondary IDs
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MIM:615980
ORDO:435660