Ontology Browser

Term:
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 10 (DOID:9004053)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
COD (Cerebroocular Dysgenesis) 
Congenital Muscular Dystrophy with Central Nervous System Involvement 
Fukuyama congenital muscular dystrophy  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 10  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 11  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 12  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 13  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 14  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 2  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 5  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 6  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 7  
Muscular Dystrophy-Dystroglycanopathy (congenital with brain and eye anomalies), Type A, 8  
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9  

Synonyms
Exact Synonyms: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 ;   MDDGA10
Primary IDs: OMIM:615041 ;   RDO:9000580

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