Human Phenotype Ontology 
Grandparent Node:
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Abnormal distal phalanx morphology of finger (HP:0009832)help
Grandparent Node:
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Sclerosis of finger phalanx (HP:0100899)help
Parent Node:
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Sclerosis of 5th finger phalanx (HP:0100921)help
Parent Node:
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Sclerosis of distal finger phalanx (HP:0100915)help
..Starting node
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Sclerosis of the distal phalanx of the 5th finger (HP:0100903)help
Term ID: 100903
Name: Sclerosis of the distal phalanx of the 5th finger
Synonym: Increased bone density in the outermost little finger bone; Increased bone density in the outermost pinkie finger bone; Increased bone density in the outermost pinky finger bone
Definition:
Comments:
Reference: HP:0100903
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the distal phalanx of the 5th finger (HP:0009243) help

 Sister Nodes: 
..expandIvory epiphyses of the distal phalanges of the hand (HP:0010252) help
..expandPatchy sclerosis of distal phalanx of finger (HP:0009840) help
..expandSclerosis of the distal phalanx of the 2nd finger (HP:0100900) help
..expandSclerosis of the distal phalanx of the 3rd finger (HP:0100901) help
..expandSclerosis of the distal phalanx of the 4th finger (HP:0100902) help
..expandSclerosis of the distal phalanx of the thumb (HP:0100912) 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:0100903HP:0100903Sclerosis of the distal phalanx of the 5th finger0 CL E G H
HP:0100903HP:0009243Patchy sclerosis of the distal 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.