Human Phenotype Ontology 
Grandparent Node:
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Abnormal 5th finger phalanx morphology (HP:0004213)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 5th finger phalanx (HP:0100921)help
..Starting node
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Patchy sclerosis of 5th finger phalanx (HP:0009377)help
Term ID: 9377
Name: Patchy sclerosis of 5th finger phalanx
Synonym: Patchy sclerosis of the phalanges of the 5th finger; Uneven increase in bone density in little finger bone; Uneven increase in bone density in pinkie finger bone; Uneven increase in bone density in pinky finger bone
Definition: Uneven increase in bone density of one or more of the phalanges of the 5th finger.
Comments:
Reference: HP:0009377
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the middle phalanx of the 5th finger (HP:0009175) help
........expandPatchy sclerosis of the proximal phalanx of the 5th finger (HP:0009231) help
........expandPatchy sclerosis of the distal phalanx of the 5th finger (HP:0009243) help

 Sister Nodes: 
..expandIvory epiphyses of the 5th finger (HP:0009388) help
..expandSclerosis of the distal phalanx of the 5th finger (HP:0100903) help
..expandSclerosis of the middle phalanx of the 5th finger (HP:0100907) help
..expandSclerosis of the proximal phalanx of the 5th finger (HP:0100911) 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:0009377HP:0009377Patchy sclerosis of 5th finger phalanx0 CL E G H
HP:0009377HP:0009243Patchy sclerosis of the distal phalanx of the 5th finger1 CL E G H
HP:0009377HP:0009231Patchy sclerosis of the proximal phalanx of the 5th finger1 CL E G H
HP:0009377HP:0009175Patchy sclerosis of the middle 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.