Human Phenotype Ontology 
Grandparent Node:
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Abnormality of toe (HP:0001780)help
Grandparent Node:
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Flexion contracture of digit (HP:0030044)help
Grandparent Node:
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Foot joint contracture (HP:0008366)help
Grandparent Node:
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obsolete Joint contractures involving the joints of the feet (HP:0100492)help
Parent Node:
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Abnormality of the 3rd toe (HP:0010320)help
Parent Node:
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Flexion contracture of toe (HP:0005830)help
..Starting node
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Flexion contracture of 3rd toe (HP:0010333)help
Term ID: 10333
Name: Flexion contracture of 3rd toe
Synonym: Joint contractures of the 3rd toe
Definition: One or more bent (flexed) joints of the third toe that cannot be straightened actively or passively.
Comments:
Reference: HP:0010333
Genes and Diseases:
 
       Child Nodes:
........expandContracture of the proximal interphalangeal joint of the 3rd toe (HP:0100349) help
........expandContracture of the distal interphalangeal joint of the 3rd toe (HP:0100353) help
........expandContracture of the metatarsophalangeal joint of the 3rd toe (HP:0100357) help

 Sister Nodes: 
..expandCamptodactyly of toe (HP:0001836) help
..expandFlexion contracture of the 2nd toe (HP:0010327) help
..expandFlexion contracture of the 4th toe (HP:0010339) help
..expandFlexion contracture of the 5th toe (HP:0010345) help
..expandFlexion contracture of the hallux (HP:0010212) 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:0010333HP:0010333Flexion contracture of 3rd toe0BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2101
HP:0010333HP:0100357Contracture of the metatarsophalangeal joint of the 3rd toe1 CL E G H
HP:0010333HP:0100353Contracture of the distal interphalangeal joint of the 3rd toe1 CL E G H
HP:0010333HP:0100349Contracture of the proximal interphalangeal joint of the 3rd toe1BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2101


Genes (1) :BCOR

Diseases (1) :OMIM:300166
 

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