Human Phenotype Ontology 
Grandparent Node:
expandAbnormal proximal phalanx morphology of the hand (HP:0009834)help
Grandparent Node:
expandSclerosis of finger phalanx (HP:0100899)help
Parent Node:
expandSclerosis of 5th finger phalanx (HP:0100921)help
Parent Node:
expandSclerosis of proximal finger phalanx (HP:0100917)help
..Starting node
..expandSclerosis of the proximal phalanx of the 5th finger (HP:0100911)help
Term ID: 100911
Name: Sclerosis of the proximal phalanx of the 5th finger
Synonym: Increased bone density in innermost little finger bone; Increased bone density in innermost pinkie finger bone; Increased bone density in innermost pinky finger bone
Definition:
Comments:
Reference: HP:0100911
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the proximal phalanx of the 5th finger (HP:0009231) help

 Sister Nodes: 
..expandIvory epiphyses of the proximal phalanges of the hand (HP:0010274) help
..expandPatchy sclerosis of proximal phalanx of finger (HP:0009856) help
..expandSclerosis of the 1st metacarpal (HP:0100914) help
..expandSclerosis of the proximal phalanx of the 2nd finger (HP:0100908) help
..expandSclerosis of the proximal phalanx of the 3rd finger (HP:0100909) help
..expandSclerosis of the proximal phalanx of the 4th finger (HP:0100910) 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:0100911HP:0100911Sclerosis of the proximal phalanx of the 5th finger0 CL E G H
HP:0100911HP:0009231Patchy sclerosis of the proximal 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.