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Ontology Browser

Term:
Congenital Muscular Dystrophy with Cerebellar Atrophy (DOID:9004366)
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Parent Terms Term With Siblings Child Terms
arthrogryposis due to muscular dystrophy  
Bethlem myopathy +   
congenital merosin-deficient muscular dystrophy 1A +   
congenital muscular dystrophy 1B 
Congenital Muscular Dystrophy associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation 
congenital muscular dystrophy due to integrin alpha-7 deficiency  
congenital muscular dystrophy due to LMNA mutation  
congenital muscular dystrophy merosin-positive 
Congenital Muscular Dystrophy plus Mental Retardation 
congenital muscular dystrophy with cataracts and intellectual disability  
Congenital Muscular Dystrophy with Cerebellar Atrophy 
Congenital Muscular Dystrophy with Rapid Progression 
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
Congenital Muscular Dystrophy, Davignon-Chauveau Type  
megaconial type congenital muscular dystrophy  
muscular dystrophy-dystroglycanopathy +   
rigid spine muscular dystrophy 1  
Ullrich congenital muscular dystrophy +   
Walker-Warburg syndrome +   

Synonyms
Primary IDs: MESH:C566392
Alternate IDs: OMIM:603323

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