Human Phenotype Ontology 
Grandparent Node:
expandAbnormal finger phalanx morphology (HP:0005918)help
Grandparent Node:
expandSclerosis of hand bone (HP:0004054)help
Parent Node:
expandAbnormality of thumb phalanx (HP:0009602)help
Parent Node:
expandSclerosis of finger phalanx (HP:0100899)help
..Starting node
..expandSclerosis of thumb phalanx (HP:0100922)help
Term ID: 100922
Name: Sclerosis of thumb phalanx
Synonym: Increased bone density in thumb bone; Sclerosis of the phalanges of the thumb
Definition:
Comments:
Reference: HP:0100922
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of thumb phalanx (HP:0009655) help
................... HP:0009634 Patchy sclerosis of the proximal phalanx of the thumb
................... HP:0009646 Patchy sclerosis of the distal phalanx of the thumb
........expandIvory epiphysis of the thumb (HP:0009692) help
................... HP:0009670 Ivory epiphysis of the proximal phalanx of the thumb
................... HP:0009681 Ivory epiphysis of the distal phalanx of the thumb
........expandSclerosis of the distal phalanx of the thumb (HP:0100912) help
................... HP:0009646 Patchy sclerosis of the distal phalanx of the thumb
........expandSclerosis of the proximal phalanx of the thumb (HP:0100913) help
................... HP:0009634 Patchy sclerosis of the proximal phalanx of the thumb

 Sister Nodes: 
..expandIvory epiphyses of the phalanges of the hand (HP:0010234) help
..expandPatchy sclerosis of finger phalanx (HP:0009772) help
..expandSclerosis of 2nd finger phalanx (HP:0100918) help
..expandSclerosis of 3rd finger phalanx (HP:0100919) help
..expandSclerosis of 4th finger phalanx (HP:0100920) help
..expandSclerosis of 5th finger phalanx (HP:0100921) help
..expandSclerosis of distal finger phalanx (HP:0100915) help
..expandSclerosis of middle finger phalanx (HP:0100916) help
..expandSclerosis of proximal finger phalanx (HP:0100917) 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:0100922HP:0100922Sclerosis of thumb phalanx0 CL E G H
HP:0100922HP:0100912Sclerosis of the distal phalanx of the thumb1 CL E G H
HP:0100922HP:0009692Ivory epiphysis of the thumb1 CL E G H
HP:0100922HP:0009655Patchy sclerosis of thumb phalanx1 CL E G H
HP:0100922HP:0100913Sclerosis of the proximal phalanx of the thumb1 CL E G H
HP:0100922HP:0009681Ivory epiphysis of the distal phalanx of the thumb2 CL E G H
HP:0100922HP:0009670Ivory epiphysis of the proximal phalanx of the thumb2 CL E G H
HP:0100922HP:0009646Patchy sclerosis of the distal phalanx of the thumb2 CL E G H
HP:0100922HP:0009634Patchy sclerosis of the proximal phalanx of the thumb2 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.