Human Phenotype Ontology 
Grandparent Node:
expandSclerosis of toe phalanx (HP:0100924)help
Parent Node:
expandAbnormal hallux phalanx morphology (HP:0010057)help
Parent Node:
expandPatchy sclerosis of toe phalanx (HP:0010178)help
Parent Node:
expandSclerosis of hallux phalanx (HP:0100930)help
..Starting node
..expandPatchy sclerosis of hallux phalanx (HP:0010063)help
Term ID: 10063
Name: Patchy sclerosis of hallux phalanx
Synonym: Patchy sclerosis of the phalanges of the hallux; Uneven increase in bone density in big toe bone
Definition: Patchy (irregular) increase in bone density of one or more phalanges of the big toe. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0010063
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the 1st metatarsal (HP:0010072) help
........expandPatchy sclerosis of the distal phalanx of the hallux (HP:0010081) help
........expandPatchy sclerosis of the proximal phalanx of the hallux (HP:0010090) help

 Sister Nodes: 
..expandSclerosis of the 1st metatarsal (HP:0100945) help
..expandSclerosis of the distal phalanx of the hallux (HP:0100944) help
..expandSclerosis of the proximal phalanx of the hallux (HP:0100943) 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:0010063HP:0010063Patchy sclerosis of hallux phalanx0 CL E G H
HP:0010063HP:0010090Patchy sclerosis of the proximal phalanx of the hallux1 CL E G H
HP:0010063HP:0010081Patchy sclerosis of the distal phalanx of the hallux1 CL E G H
HP:0010063HP:0010072Patchy sclerosis of the 1st metatarsal1 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.