Human Phenotype Ontology 
Grandparent Node:
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Sclerosis of 2nd finger phalanx (HP:0100918)help
Grandparent Node:
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Sclerosis of middle finger phalanx (HP:0100916)help
Parent Node:
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Abnormality of the middle phalanx of the 2nd finger (HP:0009543)help
Parent Node:
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Patchy sclerosis of 2nd finger phalanx (HP:0009551)help
Parent Node:
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Patchy sclerosis of middle phalanx of finger (HP:0009848)help
Parent Node:
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Sclerosis of the middle phalanx of the 2nd finger (HP:0100904)help
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Patchy sclerosis of the middle phalanx of the 2nd finger (HP:0009573)help
Term ID: 9573
Name: Patchy sclerosis of the middle phalanx of the 2nd finger
Synonym: Uneven increase in bone density in the middle bone of the index finger
Definition: Uneven (irregular) increase in bone density of the middle phalanx of the second finger.
Comments:
Reference: HP:0009573
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:0009573HP:0009573Patchy sclerosis of the middle phalanx of the 2nd 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.