Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the toes (HP:0010161)help
Grandparent Node:
expandOsteolysis involving bones of the feet (HP:0009134)help
Parent Node:
expandAbnormality of the phalanges of the 3rd toe (HP:0010330)help
Parent Node:
expandOsteolytic defects of the phalanges of the toes (HP:0010177)help
..Starting node
..expandOsteolytic defects of the phalanges of the 3rd toe (HP:0010363)help
Term ID: 10363
Name: Osteolytic defects of the phalanges of the 3rd toe
Synonym:
Definition:
Comments:
Reference: HP:0010363
Genes and Diseases:
 
       Child Nodes:
........expandOsteolytic defects of the middle phalanx of the 3rd toe (HP:0100452) help
........expandOsteolytic defects of the proximal phalanx of the 3rd toe (HP:0100455) help
........expandOsteolytic defects of the distal phalanx of the 3rd toe (HP:0100458) help

 Sister Nodes: 
..expandFoot acroosteolysis (HP:0001842) help
..expandOsteolytic defect of the proximal toe phalanx (HP:0010207) help
..expandOsteolytic defects of the distal phalanges of the toes (HP:0010189) help
..expandOsteolytic defects of the middle phalanges of the toes (HP:0010198) help
..expandOsteolytic defects of the phalanges of the 2nd toe (HP:0010351) help
..expandOsteolytic defects of the phalanges of the 4th toe (HP:0010375) help
..expandOsteolytic defects of the phalanges of the 5th toe (HP:0010387) help
..expandOsteolytic defects of the phalanges of the hallux (HP:0010062) 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:0010363HP:0010363Osteolytic defects of the phalanges of the 3rd toe0 CL E G H
HP:0010363HP:0100452Osteolytic defects of the middle phalanx of the 3rd toe1 CL E G H
HP:0010363HP:0100458Osteolytic defects of the distal phalanx of the 3rd toe1 CL E G H
HP:0010363HP:0100455Osteolytic defects of the proximal 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.