Search Ontology:
Human Disease

congenital muscular dystrophy-dystroglycanopathy type A9

Term ID
DOID:0111232
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.