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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:Tendon rupture
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Accession:HP:0100550 term browser browse the term
Definition:Breakage (tear) of a tendon.
Comment:Tendon rupture is usually painful,and accompanied by swelling, inability to move, and bunching up of the muscle normally attached to the tendon.
Synonyms:exact_synonym: Rupture of tendons;   Ruptured tendon;   Tendon/muscle rupture
 xref: SNOMEDCT_US:415749005;   UMLS:C0151937



show annotations for term's descendants           Sort by:
Tendon rupture term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G COL1A2 collagen type I alpha 2 chain IAGP HPO ORPHA:230851 NCBI chr 7:94,394,895...94,431,227
Ensembl chr 7:94,394,895...94,431,227
JBrowse link
G EMILIN1 elastin microfibril interfacer 1 IAGP HPO MIM:620080 NCBI chr 2:27,078,615...27,086,403
Ensembl chr 2:27,078,615...27,086,403
JBrowse link
G HGD homogentisate 1,2-dioxygenase IAGP HPO ORPHA:56 NCBI chr 3:120,628,172...120,682,239
Ensembl chr 3:120,628,172...120,682,269
JBrowse link
G IFIH1 interferon induced with helicase C domain 1 IAGP HPO MIM:182250 NCBI chr 2:162,267,074...162,318,684
Ensembl chr 2:162,267,074...162,318,684
JBrowse link
G TTR transthyretin IAGP HPO ORPHA:85451 NCBI chr18:31,591,877...31,598,821
Ensembl chr18:31,557,009...31,598,833
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 73897
    Phenotypic abnormality 73592
      Abnormality of the musculoskeletal system 9725
        Abnormality of the skeletal system 8610
          Abnormal skeletal morphology 8026
            Abnormal tendon morphology 1165
              Tendon rupture 5
paths to the root