Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.

Term:Myopathy
go back to main search page
Accession:HP:0003198 term browser browse the term
Definition:A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.
Comment:The diagnosis of myopathy is often confirmed on the basis of myopathic changes in muscle biopsy.
Synonyms:exact_synonym: Muscle tissue disease;   Myopathic changes
 alt_id: HP:0003569;   HP:0003705;   HP:0003742;   HP:0003802
 xref: MSH:D009135;   SNOMEDCT_US:129565002;   UMLS:C0026848



show annotations for term's descendants           Sort by:
 

Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the musculoskeletal system 0
        Abnormality of the musculature 0
          Abnormal skeletal muscle morphology 0
            Myopathy 0
              EMG: myopathic abnormalities 0
              Inflammatory myopathy 0
              Minicore myopathy + 0
              Myofibrillar myopathy 0
              Necrotizing myopathy 0
              Skeletal myopathy 0
paths to the root