ZFIN Human Disease: familial partial lipodystrophy type 6

OBO ID: DOID:0070206

Term Name:	familial partial lipodystrophy type 6		Search Ontology:
Synonyms:	familial partial lipodystrophy associated with LIPE mutations FPLD6 LIPE-related familial partial lipodystrophy LIPE-related FPLD
Definition:	A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the LIPE gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/24848981
References:	OMIM:615980 ORDO:435660
Ontology:	Human Disease ( DOID:0070206 )

Relationships

is a type of:	autosomal recessive disease familial partial lipodystrophy autosomal recessive disease familial partial lipodystrophy Show first 5 Terms

OTHER familial partial lipodystrophy type 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LIPE	lipea lipeb	Lipodystrophy, familial partial, type 6	615980

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None