Human Phenotype Ontology 
Grandparent Node:
expandAbnormal form of the vertebral bodies (HP:0003312)help
Parent Node:
expandAbnormally ossified vertebrae (HP:0100569)help
Parent Node:
expandPlatyspondyly (HP:0000926)help
..Starting node
..expandSupernumerary vertebral ossification centers (HP:0004598)help
Term ID: 4598
Name: Supernumerary vertebral ossification centers
Synonym: Supernumerary vertebral ossification centres
Definition: Three ossification sites are present in typical vertebral bodies (C3-L5): a single ossification center in the vertebral body, and one each in the two neural arches. This term applies if there are additional vertebral ossification centers present during the development and maturation of the spine.
Comments:
Reference: HP:0004598
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBiconcave flattened vertebrae (HP:0003321) help
..expandCervical platyspondyly (HP:0004558) help
..expandFlattened moderately deformed vertebrae (HP:0005752) help
..expandLumbar platyspondyly (HP:0005787) help
..expandSevere platyspondyly (HP:0004565) help
..expandSquared-off platyspondyly (HP:0008418) help
..expandThoracic platyspondyly (HP:0004592) 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:0004598HP:0004598Supernumerary vertebral ossification centers0LBR CL E G H39306518OMIM:215140Greenberg dysplasia.70
HP:0004598HP:0004598Supernumerary vertebral ossification centers0LFNG CL E G H39556560OMIM:609813Spondylocostal dysostosis 3, autosomal recessive.13


Genes (2) :LBR LFNG

Diseases (2) :OMIM:215140 OMIM:609813
 

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