Human Phenotype Ontology 
Grandparent Node:
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Abnormality of thumb phalanx (HP:0009602)help
Grandparent Node:
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Sclerosis of finger phalanx (HP:0100899)help
Parent Node:
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Abnormality of thumb epiphysis (HP:0009599)help
Parent Node:
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Ivory epiphyses of the phalanges of the hand (HP:0010234)help
Parent Node:
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Sclerosis of thumb phalanx (HP:0100922)help
..Starting node
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Ivory epiphysis of the thumb (HP:0009692)help
Term ID: 9692
Name: Ivory epiphysis of the thumb
Synonym: Increased bone density of end part of the thumb; Ivory epiphyses of the thumb
Definition: Sclerosis of one or more of the epiphyses of the thumb, leading to an increased degree of radiopacity (white or ivory appearance) in X-rays.
Comments:
Reference: HP:0009692
Genes and Diseases:
 
       Child Nodes:
........expandIvory epiphysis of the proximal phalanx of the thumb (HP:0009670) help
........expandIvory epiphysis of the distal phalanx of the thumb (HP:0009681) help

 Sister Nodes: 
..expandPatchy sclerosis of thumb phalanx (HP:0009655) help
..expandSclerosis of the distal phalanx of the thumb (HP:0100912) help
..expandSclerosis of the proximal phalanx of the thumb (HP:0100913) 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:0009692HP:0009692Ivory epiphysis of the thumb0 CL E G H
HP:0009692HP:0009681Ivory epiphysis of the distal phalanx of the thumb1 CL E G H
HP:0009692HP:0009670Ivory epiphysis of the proximal phalanx of the thumb1 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.