Human Gene Set: HP_MITOCHONDRIAL_MYOPATHY


Standard name HP_MITOCHONDRIAL_MYOPATHY
Systematic name M36392
Brief description Mitochondrial myopathy
Full description or abstract A type of myopathy associated with mitochondrial disease and characterized by findings on biopsy such as ragged red muscle fibers. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0003737
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0003737
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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