Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the middle phalanges of the toes (HP:0010183)help
Grandparent Node:
expandSclerosis of toe phalanx (HP:0100924)help
Parent Node:
expandPatchy sclerosis of toe phalanx (HP:0010178)help
Parent Node:
expandSclerosis of middle toe phalanx (HP:0100947)help
..Starting node
..expandPatchy sclerosis of middle toe phalanx (HP:0010199)help
Term ID: 10199
Name: Patchy sclerosis of middle toe phalanx
Synonym: Patchy sclerosis of the middle phalanges of the toes; Uneven increase in bone density in middle toe bone
Definition: Patchy (irregular) increase in bone density of one or more of the middle phalanges of the toes. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0010199
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the proximal phalanx of the hallux (HP:0010090) help
........expandPatchy sclerosis of the middle phalanx of the 2nd toe (HP:0010409) help
........expandPatchy sclerosis of the middle phalanx of the 3rd toe (HP:0100461) help
........expandPatchy sclerosis of the middle phalanx of the 4th toe (HP:0100462) help
........expandPatchy sclerosis of the middle phalanx of the 5th toe (HP:0100463) help

 Sister Nodes: 
..expandSclerosis of the middle phalanx of the 2nd toe (HP:0100935) help
..expandSclerosis of the middle phalanx of the 3rd toe (HP:0100936) help
..expandSclerosis of the middle phalanx of the 4th toe (HP:0100937) help
..expandSclerosis of the middle phalanx of the 5th toe (HP:0100938) 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:0010199HP:0010199Patchy sclerosis of middle toe phalanx0 CL E G H
HP:0010199HP:0010409Patchy sclerosis of the middle phalanx of the 2nd toe1 CL E G H
HP:0010199HP:0010090Patchy sclerosis of the proximal phalanx of the hallux1 CL E G H
HP:0010199HP:0100463Patchy sclerosis of the middle phalanx of the 5th toe1 CL E G H
HP:0010199HP:0100462Patchy sclerosis of the middle phalanx of the 4th toe1 CL E G H
HP:0010199HP:0100461Patchy sclerosis of the middle 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.