Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the epiphyses of the 5th toe (HP:0010341)help
Grandparent Node:
expandAbsent epiphyses of the toes (HP:0010162)help
Parent Node:
expandAbnormality of the epiphysis of the middle phalanx of the 5th toe (HP:0100098)help
Parent Node:
expandAbsent epiphyses of the 5th toe (HP:0100077)help
..Starting node
..expandAbsent epiphysis of the middle phalanx of the 5th toe (HP:0100213)help
Term ID: 100213
Name: Absent epiphysis of the middle phalanx of the 5th toe
Synonym: Absent end part of the middle bone of the little toe; Absent end part of the middle bone of the pinkie toe; Absent end part of the middle bone of the pinky toe
Definition:
Comments:
Reference: HP:0100213
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent epiphysis of the distal phalanx of the 5th toe (HP:0100202) help
..expandAbsent epiphysis of the proximal phalanx of the 5th toe (HP:0100224) 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:0100213HP:0100213Absent epiphysis 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.