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:
expandAbnormal morphology of phalanx of the 2nd toe (HP:0010324)help
Parent Node:
expandOsteolytic defects of the phalanges of the toes (HP:0010177)help
..Starting node
..expandOsteolytic defects of the phalanges of the 2nd toe (HP:0010351)help
Term ID: 10351
Name: Osteolytic defects of the phalanges of the 2nd toe
Synonym:
Definition:
Comments:
Reference: HP:0010351
Genes and Diseases:
 
       Child Nodes:
........expandOsteolytic defects of the proximal phalanx of the 2nd toe (HP:0010399) help
........expandOsteolytic defects of the middle phalanx of the 2nd toe (HP:0010408) help
........expandOsteolytic defects of the distal phalanx of the 2nd toe (HP:0010417) 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 3rd toe (HP:0010363) 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:0010351HP:0010351Osteolytic defects of the phalanges of the 2nd toe0 CL E G H
HP:0010351HP:0010417Osteolytic defects of the distal phalanx of the 2nd toe1 CL E G H
HP:0010351HP:0010408Osteolytic defects of the middle phalanx of the 2nd toe1 CL E G H
HP:0010351HP:0010399Osteolytic defects of the proximal phalanx of the 2nd 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.