Human Phenotype Ontology 
Grandparent Node:
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Sclerosis of toe phalanx (HP:0100924)help
Parent Node:
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Abnormal morphology of phalanx of the 2nd toe (HP:0010324)help
Parent Node:
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Patchy sclerosis of toe phalanx (HP:0010178)help
Parent Node:
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Sclerosis of 2nd toe phalanx (HP:0100926)help
..Starting node
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Patchy sclerosis of 2nd toe phalanx (HP:0010352)help
Term ID: 10352
Name: Patchy sclerosis of 2nd toe phalanx
Synonym: Patchy sclerosis of the phalanges of the 2nd toe; Uneven increase in bone density in 2nd toe bone
Definition: Patchy (irregular) increase in bone density of one or more of the phalanges of the second toe. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0010352
Genes and Diseases:
 
       Child Nodes:
........expandPatchy sclerosis of the proximal phalanx of the 2nd toe (HP:0010400) help
........expandPatchy sclerosis of the middle phalanx of the 2nd toe (HP:0010409) help
........expandPatchy sclerosis of the distal phalanx of the 2nd toe (HP:0010418) help

 Sister Nodes: 
..expandSclerosis of the distal phalanx of the 2nd toe (HP:0100939) help
..expandSclerosis of the middle phalanx of the 2nd toe (HP:0100935) help
..expandSclerosis of the proximal phalanx of the 2nd toe (HP:0100931) 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:0010352HP:0010352Patchy sclerosis of 2nd toe phalanx0 CL E G H
HP:0010352HP:0010418Patchy sclerosis of the distal phalanx of the 2nd toe1 CL E G H
HP:0010352HP:0010409Patchy sclerosis of the middle phalanx of the 2nd toe1 CL E G H
HP:0010352HP:0010400Patchy sclerosis of the proximal phalanx of the 2nd toe1 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.