Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the phalanges of the 2nd finger (HP:0009541)help
Grandparent Node:
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Sclerosis of finger phalanx (HP:0100899)help
Parent Node:
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Patchy sclerosis of finger phalanx (HP:0009772)help
Parent Node:
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Sclerosis of 2nd finger phalanx (HP:0100918)help
..Starting node
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Patchy sclerosis of 2nd finger phalanx (HP:0009551)help
Term ID: 9551
Name: Patchy sclerosis of 2nd finger phalanx
Synonym: Patchy sclerosis of the phalanges of the 2nd finger; Uneven increase in bone density in index finger bone
Definition: Uneven (irregular) increase in bone density of one or more of the phalanges of the 2nd finger.
Comments:
Reference: HP:0009551
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the distal phalanx of the 2nd finger (HP:0009562) help
........expandPatchy sclerosis of the middle phalanx of the 2nd finger (HP:0009573) help
........expandPatchy sclerosis of the proximal phalanx of the 2nd finger (HP:0009585) help

 Sister Nodes: 
..expandIvory epiphyses of the 2nd finger (HP:0009494) help
..expandSclerosis of the distal phalanx of the 2nd finger (HP:0100900) help
..expandSclerosis of the middle phalanx of the 2nd finger (HP:0100904) help
..expandSclerosis of the proximal phalanx of the 2nd finger (HP:0100908) 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:0009551HP:0009551Patchy sclerosis of 2nd finger phalanx0 CL E G H
HP:0009551HP:0009585Patchy sclerosis of the proximal phalanx of the 2nd finger1 CL E G H
HP:0009551HP:0009573Patchy sclerosis of the middle phalanx of the 2nd finger1 CL E G H
HP:0009551HP:0009562Patchy sclerosis of the distal phalanx of the 2nd 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.