MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
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inclusion myopathy (MONDO:0016112)
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myopathy with eye involvement (MONDO:0020259)
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myopathy, proximal, and ophthalmoplegia (MONDO:0011577)
..Starting node
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childhood-onset autosomal recessive myopathy with external ophthalmoplegia ()

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 Sister Nodes: 
..expandchildhood-onset autosomal recessive myopathy with external ophthalmoplegia ()
..expandhereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18206
Name:childhood-onset autosomal recessive myopathy with external ophthalmoplegia
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