Search Ontology:
Human Disease

autosomal recessive limb-girdle muscular dystrophy type 2P

Term ID
DOID:0110293
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
Ontology
Human Disease   ( DOID:0110293 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models