MeSH Browser

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 Numbers: 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
Revision Date: 1955/01/01

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay MeSH Supplementary Concept Data 2025