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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:Skeletal muscle atrophy
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Accession:HP:0003202 term browser browse the term
Definition:The presence of skeletal muscular atrophy (which is also known as amyotrophy).
Synonyms:exact_synonym: Amyotrophy;   Amyotrophy involving the extremities;   Muscle atrophy;   Muscle degeneration;   Muscle hypotrophy;   Muscle wasting;   Muscular atrophy;   Neurogenic muscle atrophy;   Neurogenic muscle atrophy, especially in the lower limbs;   Neurogenic muscular atrophy
 alt_id: HP:0001299;   HP:0003545;   HP:0003671;   HP:0003702;   HP:0003746;   HP:0006995;   HP:0007171;   HP:0007356;   HP:0009010;   HP:0009048;   HP:0100868
 xref: SNOMEDCT_US:74035001;   UMLS:C0234958;   UMLS:C0270948;   UMLS:C0541794;   UMLS:C1843479


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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the musculoskeletal system 0
        Abnormality of the musculature 0
          Abnormal skeletal muscle morphology 0
            Skeletal muscle atrophy 0
              Distal amyotrophy + 0
              Generalized amyotrophy + 0
              Limb-girdle muscle atrophy + 0
              Lower limb amyotrophy + 0
              Nonprogressive muscular atrophy 0
              Pectoralis amyotrophy 0
              Peroneal muscle atrophy 0
              Proximal amyotrophy + 0
              Scapuloperoneal amyotrophy 0
              Spinal muscular atrophy + 0
              Sternocleidomastoid amyotrophy 0
              Upper limb amyotrophy + 0
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