Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the 3rd toe (HP:0010330)help
Grandparent Node:
expandDuplication of phalanx of toe (HP:0010181)help
Parent Node:
expandAbnormality of the middle phalanx of the 3rd toe (HP:0010369)help
Parent Node:
expandDuplication of middle phalanx of toe (HP:0010202)help
Parent Node:
expandDuplication of phalanx of the 3rd toe (HP:0010367)help
..Starting node
..expandDuplication of the middle phalanx of the 3rd toe (HP:0100401)help
Term ID: 100401
Name: Duplication of the middle phalanx of the 3rd toe
Synonym: Duplication of the middle bone of the 3rd toe; Duplication of the middle phalanx of the third toe; Partial/complete duplication of the middle phalanx of the 3rd toe
Definition: Partial or complete duplication of middle phalanx of third toe.
Comments:
Reference: HP:0100401
Genes and Diseases:
 
       Child Nodes:
........expandComplete duplication of the middle phalanx of the 3rd toe (HP:0100410) help
........expandPartial duplication of the middle phalanx of the 3rd toe (HP:0100419) help

 Sister Nodes: 
..expandDuplication of the distal phalanx of the 3rd toe (HP:0100398) help
..expandDuplication of the proximal phalanx of the 3rd toe (HP:0100404) 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:0100401HP:0100401Duplication of the middle phalanx of the 3rd toe0 CL E G H
HP:0100401HP:0100419Partial duplication of the middle phalanx of the 3rd toe1 CL E G H
HP:0100401HP:0100410Complete duplication of the middle phalanx of the 3rd toe1 CL E G H


Genes (0) :

Diseases (0) :
 

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