Human Gene Set: HP_EMG_MYOPATHIC_ABNORMALITIES


Standard name HP_EMG_MYOPATHIC_ABNORMALITIES
Systematic name M36312
Brief description EMG: myopathic abnormalities
Full description or abstract The presence of abnormal electromyographic patterns indicative of myopathy, such as small-short polyphasic motor unit potentials. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0003458
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External links https://hpo.jax.org/app/browse/term/HP:0003458
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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
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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