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Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay MeSH Supplementary Concept Data 2022


MeSH Supplementary
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
Unique ID
C567769
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567769
Entry Term(s)
Mitochondrial Complex Deficiency, Combined
Myopathy With Cataract And Combined Respiratory Chain Deficiency
Registry Number
0
Heading Mapped to
*Cataract
Developmental Disabilities
*Mitochondrial Myopathies
*Hearing Loss
Frequency
1
Note
asociated with mutation in GFER
Date of Entry
2012/08/24
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Preferred
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