Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cartilage morphology (HP:0002763)help
Grandparent Node:
expandEctopic calcification (HP:0010766)help
Parent Node:
expandAbnormal rib ossification (HP:0012306)help
Parent Node:
expandCalcification of cartilage (HP:0100593)help
..Starting node
..expandCostal cartilage calcification (HP:0006646)help
Term ID: 6646
Name: Costal cartilage calcification
Synonym: Cartilaginous ossification of rib
Definition: Calcification of the costal cartilages, which are bars of hyaline cartilage found at the anterior ends of the ribs which serve to prolong the ribs forward and contribute to the elasticity of the walls of the thorax.
Comments:
Reference: HP:0006646
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalcification of the auricular cartilage (HP:0005103) help
..expandProgressive calcification of costochondral cartilage (HP:0006600) help
..expandStippled chondral calcification (HP:0002764) 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:0006646HP:0006646Costal cartilage calcification0LBR CL E G H39306518OMIM:215140Greenberg dysplasia70
HP:0006646HP:0006646Costal cartilage calcification0MGP CL E G H42567060OMIM:245150Keutel syndrome.33
HP:0006646HP:0006646Costal cartilage calcification0SLC26A2 CL E G H183610994OMIM:222600Diastrophic dysplasia.166


Genes (3) :LBR MGP SLC26A2

Diseases (3) :OMIM:215140 OMIM:245150 OMIM:222600
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.