Human Phenotype Ontology 
Grandparent Node:
expandAbnormal middle phalanx morphology of the hand (HP:0009833)help
Grandparent Node:
expandSclerosis of finger phalanx (HP:0100899)help
Parent Node:
expandSclerosis of 5th finger phalanx (HP:0100921)help
Parent Node:
expandSclerosis of middle finger phalanx (HP:0100916)help
..Starting node
..expandSclerosis of the middle phalanx of the 5th finger (HP:0100907)help
Term ID: 100907
Name: Sclerosis of the middle phalanx of the 5th finger
Synonym: Increased bone density in the middle bone of the little finger; Increased bone density in the middle bone of the pinkie finger; Increased bone density in the middle bone of the pinky finger
Definition:
Comments:
Reference: HP:0100907
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the middle phalanx of the 5th finger (HP:0009175) help

 Sister Nodes: 
..expandIvory epiphyses of the middle phalanges of the hand (HP:0010263) help
..expandPatchy sclerosis of middle phalanx of finger (HP:0009848) help
..expandSclerosis of the middle phalanx of the 2nd finger (HP:0100904) help
..expandSclerosis of the middle phalanx of the 3rd finger (HP:0100905) help
..expandSclerosis of the middle phalanx of the 4th finger (HP:0100906) 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:0100907HP:0100907Sclerosis of the middle phalanx of the 5th finger0 CL E G H
HP:0100907HP:0009175Patchy sclerosis of the middle phalanx of the 5th finger1 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.