Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the distal phalanges of the toes (HP:0010182)help
Grandparent Node:
expandSclerosis of toe phalanx (HP:0100924)help
Parent Node:
expandSclerosis of 5th toe phalanx (HP:0100929)help
Parent Node:
expandSclerosis of distal toe phalanx (HP:0100948)help
..Starting node
..expandSclerosis of the distal phalanx of the 5th toe (HP:0100942)help
Term ID: 100942
Name: Sclerosis of the distal phalanx of the 5th toe
Synonym: Increased bone density in the outermost bone of the little toe; Increased bone density in the outermost bone of the pinkie toe; Increased bone density in the outermost bone of the pinky toe
Definition:
Comments:
Reference: HP:0100942
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the distal phalanx of the 5th toe (HP:0100469) help

 Sister Nodes: 
..expandPatchy sclerosis of distal toe phalanx (HP:0010190) help
..expandSclerosis of the distal phalanx of the 2nd toe (HP:0100939) help
..expandSclerosis of the distal phalanx of the 3rd toe (HP:0100940) help
..expandSclerosis of the distal phalanx of the 4th toe (HP:0100941) help
..expandSclerosis of the distal phalanx of the hallux (HP:0100944) 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:0100942HP:0100942Sclerosis of the distal phalanx of the 5th toe0 CL E G H
HP:0100942HP:0100469Patchy sclerosis of the distal phalanx of the 5th 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.