ZFIN Human Disease: autosomal recessive limb-girdle muscular dystrophy type 2W

OBO ID: DOID:0110288

Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2W		Search Ontology:
Synonyms:	LGMD2W muscular dystrophy, limb-girdle, type 2W
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14. (2)
References:	OMIM:616827 ORDO:466801
Ontology:	Human Disease ( DOID:0110288 )

Relationships

is a type of:	autosomal recessive limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy Show first 5 Terms

OTHER autosomal recessive limb-girdle muscular dystrophy type 2W PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LIMS2	lims2	?Muscular dystrophy, autosomal recessive, with cardiomyopathy and triangular tongue	616827

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None