Human Phenotype Ontology 
Grandparent Node:
expandSclerosis of toe phalanx (HP:0100924)help
Parent Node:
expandAbnormality of the phalanges of the 5th toe (HP:0010342)help
Parent Node:
expandPatchy sclerosis of toe phalanx (HP:0010178)help
Parent Node:
expandSclerosis of 5th toe phalanx (HP:0100929)help
..Starting node
..expandPatchy sclerosis of 5th toe phalanx (HP:0010388)help
Term ID: 10388
Name: Patchy sclerosis of 5th toe phalanx
Synonym: Patchy sclerosis of the phalanges of the 5th toe; Uneven increase in bone density in little toe bone; Uneven increase in bone density in pinkie toe bone; Uneven increase in bone density in pinky toe bone
Definition: Patchy (irregular) increase in bone density of one or more of the phalanges of the fifth toe. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0010388
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the middle phalanx of the 5th toe (HP:0100463) help
........expandPatchy sclerosis of the proximal phalanx of the 5th toe (HP:0100466) help
........expandPatchy sclerosis of the distal phalanx of the 5th toe (HP:0100469) help

 Sister Nodes: 
..expandSclerosis of the distal phalanx of the 5th toe (HP:0100942) help
..expandSclerosis of the middle phalanx of the 5th toe (HP:0100938) help
..expandSclerosis of the proximal phalanx of the 5th toe (HP:0100934) 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:0010388HP:0010388Patchy sclerosis of 5th toe phalanx0 CL E G H
HP:0010388HP:0100466Patchy sclerosis of the proximal phalanx of the 5th toe1 CL E G H
HP:0010388HP:0100463Patchy sclerosis of the middle phalanx of the 5th toe1 CL E G H
HP:0010388HP: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.