Human Phenotype Ontology 
Grandparent Node:
expandSclerosis of 5th finger phalanx (HP:0100921)help
Grandparent Node:
expandSclerosis of middle finger phalanx (HP:0100916)help
Parent Node:
expandAbnormality of the middle phalanx of the 5th finger (HP:0004219)help
Parent Node:
expandPatchy sclerosis of 5th finger phalanx (HP:0009377)help
Parent Node:
expandPatchy sclerosis of middle phalanx of finger (HP:0009848)help
Parent Node:
expandSclerosis of the middle phalanx of the 5th finger (HP:0100907)help
..Starting node
..expandPatchy sclerosis of the middle phalanx of the 5th finger (HP:0009175)help
Term ID: 9175
Name: Patchy sclerosis of the middle phalanx of the 5th finger
Synonym: Uneven increase in bone density in the middle bone of the little finger; Uneven increase in bone density in the middle bone of the pinkie finger; Uneven increase in bone density in the middle bone of the pinky finger
Definition: Patchy increase in bone density of the middle phalanx of the 5th finger.
Comments:
Reference: HP:0009175
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:0009175HP:0009175Patchy sclerosis of the middle 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.