Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the hand (HP:0001155)help
Grandparent Node:
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Abnormality of upper limb joint (HP:0009810)help
Grandparent Node:
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Upper-limb joint contracture (HP:0100360)help
Parent Node:
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Joint contracture of the hand (HP:0009473)help
..Starting node
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Dupuytren contracture (HP:0005679)help
Term ID: 5679
Name: Dupuytren contracture
Synonym:
Definition: An abnormality of the hand resulting from contracture of the palmar fascia with a fixed flexion deformity of the metacarpophalangeal (MCP) joints and the proximal interphalangeal (PIP) joints.
Comments:
Reference: HP:0005679
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBethlem sign (HP:0030233) help
..expandFlexion contracture of finger (HP:0012785) 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:0005679HP:0005679Dupuytren contracture0KIF5A CL E G H37986323ORPHA:100991Autosomal dominant spastic paraplegia type 10HP:0040283 - Occasional93


Genes (1) :KIF5A

Diseases (1) :ORPHA:100991
 

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