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DO Term : familial partial lipodystrophy type 6 [DOID:0070206] 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 LIPE gene on chromosome 19q13.
  • synonyms:
  • ORDO:435660,
  • LIPE-related familial partial lipodystrophy,
  • LIPE-related FPLD,
  • 615980,
  • FPLD6,
  • familial partial lipodystrophy associated with LIPE mutations,
  • OMIM:615980
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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