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

OBO ID: DOID:0110293

Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2P		Search Ontology:
Synonyms:	LGMD2P MDDGC9 muscular dystrophy-dystroglycanopathy (limb-girdle) type C9 muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/21388311
References:	ICD10CM:G71.0 OMIM:613818 ORDO:280333
Ontology:	Human Disease ( DOID:0110293 )

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 2P PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DAG1	dag1	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9	613818

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None