Human Phenotype Ontology 
Grandparent Node:
expandSclerosis of 4th toe phalanx (HP:0100928)help
Grandparent Node:
expandSclerosis of middle toe phalanx (HP:0100947)help
Parent Node:
expandPatchy sclerosis of 4th toe phalanx (HP:0010376)help
Parent Node:
expandPatchy sclerosis of middle toe phalanx (HP:0010199)help
Parent Node:
expandSclerosis of the middle phalanx of the 4th toe (HP:0100937)help
..Starting node
..expandPatchy sclerosis of the middle phalanx of the 4th toe (HP:0100462)help
Term ID: 100462
Name: Patchy sclerosis of the middle phalanx of the 4th toe
Synonym: Uneven increase in bone density in middle bone of the 4th toe
Definition: Uneven increase in bone density of the middle phalanx of the fourth toe. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0100462
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100462HP:0100462Patchy sclerosis of the middle phalanx of the 4th 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.