Human Phenotype Ontology 
Grandparent Node:
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Sclerosis of 4th toe phalanx (HP:0100928)help
Grandparent Node:
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Sclerosis of proximal toe phalanx (HP:0100946)help
Parent Node:
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Patchy sclerosis of 4th toe phalanx (HP:0010376)help
Parent Node:
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Patchy sclerosis of proximal toe phalanx (HP:0010208)help
Parent Node:
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Sclerosis of the proximal phalanx of the 4th toe (HP:0100933)help
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Patchy sclerosis of the proximal phalanx of the 4th toe (HP:0100465)help
Term ID: 100465
Name: Patchy sclerosis of the proximal phalanx of the 4th toe
Synonym: Uneven increase in bone density in the innermost bone of the 4th toe
Definition: Uneven increase in bone density of the proximal phalanx of the fourth toe. This can take on many forms depending on severity and distribution as can be seen on x-rays.
Comments:
Reference: HP:0100465
Genes and Diseases:
 
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InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100465HP:0100465Patchy sclerosis of the proximal phalanx of the 4th toe0 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.