Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the epiphyses of the middle phalanges of the hand (HP:0010244)help
Grandparent Node:
expandIvory epiphyses of the phalanges of the hand (HP:0010234)help
Grandparent Node:
expandSclerosis of middle finger phalanx (HP:0100916)help
Parent Node:
expandAbnormality of the epiphysis of the middle phalanx of the 4th finger (HP:0009247)help
Parent Node:
expandIvory epiphyses of the 4th finger (HP:0009399)help
Parent Node:
expandIvory epiphyses of the middle phalanges of the hand (HP:0010263)help
..Starting node
..expandIvory epiphysis of the middle phalanx of the 4th finger (HP:0009220)help
Term ID: 9220
Name: Ivory epiphysis of the middle phalanx of the 4th finger
Synonym: Increased bone density of end part of the middle ring finger bone
Definition: Sclerosis of the epiphysis of the middle phalanx of the ring finger, leading to an increased degree of radiopacity (white or ivory appearance) in X-rays.
Comments:
Reference: HP:0009220
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIvory epiphysis of the middle phalanx of the 2nd finger (HP:0009519) help
..expandIvory epiphysis of the middle phalanx of the 3rd finger (HP:0009327) help
..expandIvory epiphysis of the middle phalanx of the 5th finger (HP:0009209) help
..expandIvory epiphysis of the proximal phalanx of the thumb (HP:0009670) 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:0009220HP:0009220Ivory epiphysis of the middle phalanx of the 4th finger0 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.