Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the middle phalanx of the 5th toe (HP:0010393)help
Grandparent Node:
expandDuplication of middle phalanx of toe (HP:0010202)help
Grandparent Node:
expandDuplication of the phalanges of the 5th toe (HP:0010391)help
Parent Node:
expandDuplication of the middle phalanx of the 5th toe (HP:0100403)help
..Starting node
..expandComplete duplication of the middle phalanx of the 5th toe (HP:0100412)help
Term ID: 100412
Name: Complete duplication of the middle phalanx of the 5th toe
Synonym: Complete duplication of the middle bone of the little toe; Complete duplication of the middle bone of the pinkie toe; Complete duplication of the middle bone of the pinky toe; Complete duplication of the middle phalanx of the fifth toe
Definition: Complete duplication of the middle phalanx of the 5th toe.
Comments:
Reference: HP:0100412
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPartial duplication of the middle phalanx of the 5th toe (HP:0100421) 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:0100412HP:0100412Complete duplication of the middle phalanx of the 5th toe0 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.