Human Phenotype Ontology 
Grandparent Node:
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Abnormal rib morphology (HP:0000772)help
Parent Node:
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Abnormality of the costochondral junction (HP:0000919)help
..Starting node
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Costochondral joint sclerosis (HP:0006623)help
Term ID: 6623
Name: Costochondral joint sclerosis
Synonym: Sclerotic costochondral joints
Definition: Abnormal increase in density of the tissue at the costochondral junctions.
Comments:
Reference: HP:0006623
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBulging of the costochondral junction (HP:0000893) help
..expandCostochondral pain (HP:0006649) help
..expandEnlargement of the costochondral junction (HP:0000920) help
..expandIrregular chondrocostal junctions (HP:0006606) help
..expandPrecocious costochondral ossification (HP:0006607) help
..expandProgressive calcification of costochondral cartilage (HP:0006600) help
..expandRachitic rosary (HP:0000897) help
..expandWide-cupped costochondral junctions (HP:0000910) 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:0006623HP:0006623Costochondral joint sclerosis0 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.