Human Phenotype Ontology 
Grandparent Node:
expandAbnormal hallux phalanx morphology (HP:0010057)help
Grandparent Node:
expandDuplication of phalanx of toe (HP:0010181)help
Parent Node:
expandAbnormal morphology of the proximal phalanx of the hallux (HP:0010052)help
Parent Node:
expandDuplication of middle phalanx of toe (HP:0010202)help
Parent Node:
expandDuplication of phalanx of hallux (HP:0010066)help
..Starting node
..expandDuplication of the proximal phalanx of the hallux (HP:0010093)help
Term ID: 10093
Name: Duplication of the proximal phalanx of the hallux
Synonym: Duplication of the innermost bone of big toe
Definition: Partial or complete duplication of the proximal phalanx of big toe.
Comments:
Reference: HP:0010093
Genes and Diseases:
 
       Child Nodes:
........expandComplete duplication of the proximal phalanx of the hallux (HP:0010094) help
........expandPartial duplication of the proximal phalanx of the hallux (HP:0010095) help

 Sister Nodes: 
..expandComplete duplication of hallux phalanx (HP:0010100) help
..expandDuplication of the distal phalanx of the hallux (HP:0010084) help
..expandPartial duplication of the phalanges of the hallux (HP:0010101) 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:0010093HP:0010093Duplication of the proximal phalanx of the hallux0RAB23 CL E G H5171514263OMIM:201000Carpenter syndrome 131
HP:0010093HP:0010095Partial duplication of the proximal phalanx of the hallux1 CL E G H
HP:0010093HP:0010094Complete duplication of the proximal phalanx of the hallux1 CL E G H


Genes (1) :RAB23

Diseases (1) :OMIM:201000
 

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