Human Phenotype Ontology 
Grandparent Node:
expandSclerosis of 5th finger phalanx (HP:0100921)help
Grandparent Node:
expandSclerosis of proximal finger phalanx (HP:0100917)help
Parent Node:
expandAbnormality of the proximal phalanx of the 5th finger (HP:0009150)help
Parent Node:
expandPatchy sclerosis of 5th finger phalanx (HP:0009377)help
Parent Node:
expandPatchy sclerosis of proximal phalanx of finger (HP:0009856)help
Parent Node:
expandSclerosis of the proximal phalanx of the 5th finger (HP:0100911)help
..Starting node
..expandPatchy sclerosis of the proximal phalanx of the 5th finger (HP:0009231)help
Term ID: 9231
Name: Patchy sclerosis of the proximal phalanx of the 5th finger
Synonym: Uneven increase in bone density in the innermost bone of little finger; Uneven increase in bone density in the innermost bone of pinkie finger; Uneven increase in bone density in the innermost bone of pinky finger
Definition: Patchy increase in bone density of the proximal phalanx of the 5th finger.
Comments:
Reference: HP:0009231
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009231HP:0009231Patchy sclerosis of the proximal phalanx of the 5th 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.