Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of toe proximal phalanx (HP:0010184)help
Grandparent Node:
expandSclerosis of toe phalanx (HP:0100924)help
Parent Node:
expandSclerosis of 3rd toe phalanx (HP:0100927)help
Parent Node:
expandSclerosis of proximal toe phalanx (HP:0100946)help
..Starting node
..expandSclerosis of the proximal phalanx of the 3rd toe (HP:0100932)help
Term ID: 100932
Name: Sclerosis of the proximal phalanx of the 3rd toe
Synonym: Increased bone density in the innermost bone of the 3rd toe
Definition: An elevation in bone density in the proximal phalanx of the third toe. Sclerosis is normally detected on a radiograph as an area of increased opacity.
Comments:
Reference: HP:0100932
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the proximal phalanx of the 3rd toe (HP:0100464) help

 Sister Nodes: 
..expandPatchy sclerosis of proximal toe phalanx (HP:0010208) help
..expandSclerosis of the proximal phalanx of the 2nd toe (HP:0100931) help
..expandSclerosis of the proximal phalanx of the 4th toe (HP:0100933) help
..expandSclerosis of the proximal phalanx of the 5th toe (HP:0100934) 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:0100932HP:0100932Sclerosis of the proximal phalanx of the 3rd toe0 CL E G H
HP:0100932HP:0100464Patchy sclerosis 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.