Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the phalanges of the toes (HP:0010161)help
Grandparent Node:
expandSclerosis of foot bone (HP:0100925)help
Parent Node:
expandSclerosis of toe phalanx (HP:0100924)help
..Starting node
..expandSclerosis of hallux phalanx (HP:0100930)help
Term ID: 100930
Name: Sclerosis of hallux phalanx
Synonym: Increased bone density in big toe bone; Sclerosis of the phalanges of the hallux
Definition: An elevation in bone density in one or more phalanges of the big toe. Sclerosis is normally detected on a radiograph as an area of increased opacity.
Comments:
Reference: HP:0100930
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of hallux phalanx (HP:0010063) help
................... HP:0010072 Patchy sclerosis of the 1st metatarsal
................... HP:0010081 Patchy sclerosis of the distal phalanx of the hallux
................... HP:0010090 Patchy sclerosis of the proximal phalanx of the hallux
........expandSclerosis of the proximal phalanx of the hallux (HP:0100943) help
................... HP:0010090 Patchy sclerosis of the proximal phalanx of the hallux
........expandSclerosis of the distal phalanx of the hallux (HP:0100944) help
................... HP:0010081 Patchy sclerosis of the distal phalanx of the hallux
........expandSclerosis of the 1st metatarsal (HP:0100945) help
................... HP:0010072 Patchy sclerosis of the 1st metatarsal

 Sister Nodes: 
..expandPatchy sclerosis of toe phalanx (HP:0010178) help
..expandSclerosis of 2nd toe phalanx (HP:0100926) help
..expandSclerosis of 3rd toe phalanx (HP:0100927) help
..expandSclerosis of 4th toe phalanx (HP:0100928) help
..expandSclerosis of 5th toe phalanx (HP:0100929) help
..expandSclerosis of distal toe phalanx (HP:0100948) help
..expandSclerosis of middle toe phalanx (HP:0100947) help
..expandSclerosis of proximal toe phalanx (HP:0100946) 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:0100930HP:0100930Sclerosis of hallux phalanx0 CL E G H
HP:0100930HP:0010063Patchy sclerosis of hallux phalanx1 CL E G H
HP:0100930HP:0100945Sclerosis of the 1st metatarsal1 CL E G H
HP:0100930HP:0100944Sclerosis of the distal phalanx of the hallux1 CL E G H
HP:0100930HP:0100943Sclerosis of the proximal phalanx of the hallux1 CL E G H
HP:0100930HP:0010090Patchy sclerosis of the proximal phalanx of the hallux2 CL E G H
HP:0100930HP:0010081Patchy sclerosis of the distal phalanx of the hallux2 CL E G H
HP:0100930HP:0010072Patchy sclerosis of the 1st metatarsal2 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.