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DO Term : familial partial lipodystrophy type 5 [DOID:0070203] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
ORDO:435651,
FPLD5,
CIDEC-related FPLD,
familial partial lipodystrophy associated with CIDEC mutations,
615238,
OMIM:615238

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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