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Ontology Browser

Term:
congenital muscular dystrophy-dystroglycanopathy type A10 (DOID:0111239)
Annotations: Rat: (1) Mouse: (1) Human: (2) 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  
A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2. (DO)
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  
Fukuyama congenital muscular dystrophy  

Synonyms
Exact Synonyms: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 ;   MDDGA10 ;   Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 10
Primary IDs: OMIM:615041
Alternate IDs: RDO:9000580
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/23217329

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.