Human Phenotype Ontology 
Grandparent Node:
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Abnormal hallux phalanx morphology (HP:0010057)help
Grandparent Node:
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Duplication of phalanx of toe (HP:0010181)help
Parent Node:
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Duplication of phalanx of hallux (HP:0010066)help
..Starting node
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Partial duplication of the phalanges of the hallux (HP:0010101)help
Term ID: 10101
Name: Partial duplication of the phalanges of the hallux
Synonym: Partial duplication of big toe; partial duplication of hallux
Definition:
Comments:
Reference: HP:0010101
Genes and Diseases:
 
       Child Nodes:
........expandPartial duplication of the proximal phalanx of the hallux (HP:0010095) help
........expandPartial duplication of the distal phalanx of the hallux (HP:0010097) help
........expandPartial duplication of the 1st metatarsal (HP:0010099) help

 Sister Nodes: 
..expandComplete duplication of hallux phalanx (HP:0010100) help
..expandDuplication of the distal phalanx of the hallux (HP:0010084) help
..expandDuplication of the proximal phalanx of the hallux (HP:0010093) 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:0010101HP:0010101Partial duplication of the phalanges of the hallux0CANT1 CL E G H12458319721OMIM:251450Desbuquois dysplasia 185
HP:0010101HP:0010099Partial duplication of the 1st metatarsal1 CL E G H
HP:0010101HP:0010095Partial duplication of the proximal phalanx of the hallux1 CL E G H
HP:0010101HP:0010097Partial duplication of the distal phalanx of the hallux1CANT1 CL E G H12458319721OMIM:251450Desbuquois dysplasia 1.85


Genes (1) :CANT1

Diseases (1) :OMIM:251450
 

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