ZFIN Human Disease: familial partial lipodystrophy type 5

OBO ID: DOID:0070203

Term Name:	familial partial lipodystrophy type 5		Search Ontology:
Synonyms:	CIDEC-related FPLD familial partial lipodystrophy associated with CIDEC mutations FPLD5
Definition:	A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the CIDEC gene on chromosome 3p25. https://www.ncbi.nlm.nih.gov/pubmed/20049731
References:	OMIM:615238 ORDO:435651
Ontology:	Human Disease ( DOID:0070203 )

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 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CIDEC	cidec	?Lipodystrophy, familial partial, type 5	615238

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None