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:
Ontology: Human Disease   (DOID:0110293)
OTHER autosomal recessive limb-girdle muscular dystrophy type 2P PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DAG1 Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9 613818
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None