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Ontology Browser

Term:
congenital muscular dystrophy-dystroglycanopathy type A9 (DOID:0111232)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
congenital muscular dystrophy-dystroglycanopathy A14  
congenital muscular dystrophy-dystroglycanopathy A7  
congenital muscular dystrophy-dystroglycanopathy type A1  
congenital muscular dystrophy-dystroglycanopathy type A10  
congenital muscular dystrophy-dystroglycanopathy type A11  
congenital muscular dystrophy-dystroglycanopathy type A12  
congenital muscular dystrophy-dystroglycanopathy type A13  
congenital muscular dystrophy-dystroglycanopathy type A2  
congenital muscular dystrophy-dystroglycanopathy type A3  
congenital muscular dystrophy-dystroglycanopathy type A5  
congenital muscular dystrophy-dystroglycanopathy type A6  
congenital muscular dystrophy-dystroglycanopathy type A8  
congenital muscular dystrophy-dystroglycanopathy type A9  
A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31. (DO)
Fukuyama congenital muscular dystrophy  

Synonyms
Exact Synonyms: MDDGA9 ;   Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), type A, 9 ;   WALKER-WARBURG SYNDROME OR MUSCLE-EYE BRAIN DISEASE, DAG1-RELATED ;   congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
Primary IDs: OMIM:616538
Alternate IDs: RDO:9001467
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/24052401 "DO"

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