Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abnormality of connective tissue (HP:0003549)help
..Starting node
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Musculotendinous retraction (HP:0031462)help
Term ID: 31462
Name: Musculotendinous retraction
Synonym:
Definition: Abnormal reduction in length of a tendon which tends to pull (retract) the attached muscle tissue with shortening of the muscle fibers often accompanied by atrophy and fatty degeneration of the affected muscle tissue.
Comments:
Reference: HP:0031462
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal adipose tissue morphology (HP:0009124) help
..expandAbnormal mast cell morphology (HP:0100494) help
..expandAbnormal odontoid tissue morphology (HP:3000050) help
..expandAbnormal Sharpey fiber morphology (HP:0100685) help
..expandAbnormality of the fascia (HP:0100536) help
..expandCellulitis (HP:0100658) help
..expandCongenital mesoblastic nephroma (HP:0100881) help
..expandConnective tissue nevi (HP:0100898) help
..expandFlexion contracture (HP:0001371) help
..expandHernia (HP:0100790) help
..expandIncreased connective tissue (HP:0009025) help
..expandScarring (HP:0100699) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031462HP:0031462Musculotendinous retraction0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.