Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the phalanges of the toes (HP:0010161)help
Grandparent Node:
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Osteolysis involving bones of the feet (HP:0009134)help
Parent Node:
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Abnormality of the phalanges of the 4th toe (HP:0010336)help
Parent Node:
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Osteolytic defects of the phalanges of the toes (HP:0010177)help
..Starting node
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Osteolytic defects of the phalanges of the 4th toe (HP:0010375)help
Term ID: 10375
Name: Osteolytic defects of the phalanges of the 4th toe
Synonym:
Definition:
Comments:
Reference: HP:0010375
Genes and Diseases:
 
       Child Nodes:
........expandOsteolytic defects of the middle phalanx of the 4th toe (HP:0100453) help
........expandOsteolytic defects of the proximal phalanx of the 4th toe (HP:0100456) help
........expandOsteolytic defects of the distal phalanx of the 4th toe (HP:0100459) 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 3rd toe (HP:0010363) 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:0010375HP:0010375Osteolytic defects of the phalanges of the 4th toe0 CL E G H
HP:0010375HP:0100459Osteolytic defects of the distal phalanx of the 4th toe1 CL E G H
HP:0010375HP:0100456Osteolytic defects of the proximal phalanx of the 4th toe1 CL E G H
HP:0010375HP:0100453Osteolytic defects of the middle phalanx of the 4th 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.