Human Phenotype Ontology 
Grandparent Node:
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Limb joint contracture (HP:0003121)help
Parent Node:
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Lower-limb joint contracture (HP:0005750)help
..Starting node
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Hamstring contractures (HP:0003089)help
Term ID: 3089
Name: Hamstring contractures
Synonym: Hamstring contractures
Definition:
Comments:
Reference: HP:0003089
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAdductor longus contractures (HP:0006366) help
..expandAnkle flexion contracture (HP:0006466) help
..expandCongenital foot contractures (HP:0005745) help
..expandFoot joint contracture (HP:0008366) help
..expandHip contracture (HP:0003273) help
..expandKnee flexion contracture (HP:0006380) 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:0003089HP:0003089Hamstring contractures0ABCD1 CL E G H21561ORPHA:139396X-linked cerebral adrenoleukodystrophyHP:0040283 - Occasional135
HP:0003089HP:0003089Hamstring contractures0ACTA1 CL E G H58129ORPHA:97244Rigid spine syndromeHP:0040282 - Frequent96
HP:0003089HP:0003089Hamstring contractures0ANO5 CL E G H20385927337ORPHA:206549Anoctamin-5-related limb-girdle muscular dystrophy R12HP:0040283 - Occasional304
HP:0003089HP:0003089Hamstring contractures0CAPN3 CL E G H8251480ORPHA:267Calpain-3-related limb-girdle muscular dystrophy R1HP:0040282 - Frequent323
HP:0003089HP:0003089Hamstring contractures0DMD CL E G H17562928OMIM:310200Duchenne muscular dystrophy1496
HP:0003089HP:0003089Hamstring contractures0FHL1 CL E G H22733702OMIM:300696Myopathy, X-linked, with postural muscle atrophy68
HP:0003089HP:0003089Hamstring contractures0OPA1 CL E G H49768140OMIM:210000Behr syndrome.214
HP:0003089HP:0003089Hamstring contractures0SELENON CL E G H5719015999ORPHA:97244Rigid spine syndromeHP:0040282 - Frequent144


Genes (8) :ABCD1 ACTA1 ANO5 CAPN3 DMD FHL1 OPA1 SELENON

Diseases (7) :ORPHA:139396 ORPHA:97244 ORPHA:206549 ORPHA:267 OMIM:310200 OMIM:300696 OMIM:210000
 

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