OBO ID: DOID:0111232
Term Name: congenital muscular dystrophy-dystroglycanopathy type A9 Search Ontology:
Synonyms:
  • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
  • MDDGA9
  • Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
Definition: A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31. https://www.ncbi.nlm.nih.gov/pubmed/24052401
References:
Ontology: Human Disease   ( DOID:0111232 )
OTHER congenital muscular dystrophy-dystroglycanopathy type A9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DAG1 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9 616538
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None