Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vertebral morphology (HP:0003468)help
Parent Node:
expandAbnormal form of the vertebral bodies (HP:0003312)help
..Starting node
..expandTrapezoidal vertebral body (HP:0005621)help
Term ID: 5621
Name: Trapezoidal vertebral body
Synonym: Trapezoidal shaped vertebral bodies; Trapezoidal vertebral bodies
Definition: An anomalous trapezoidal appearance of a vertebral body. A trapezoid is a four-sided shape that has two sides that are parallel and two sides that are not parallel. In this case, the two lateral sides of the vertebra are parallel, and the top and the bottom are slanted with respect to each other such that the vertebra is shorter in the fron or back than on the other side.
Comments:
Reference: HP:0005621
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of spinal facet joint (HP:0030870) help
..expandAbnormality of the vertebral endplates (HP:0005106) help
..expandAbnormality of the vertebral spinous processes (HP:0008516) help
..expandAnisospondyly (HP:0002879) help
..expandAnterior concavity of thoracic vertebrae (HP:0004611) help
..expandBeaking of vertebral bodies (HP:0004568) help
..expandBiconcave vertebral bodies (HP:0004586) help
..expandBiconvex vertebral bodies (HP:0004625) help
..expandBifid thoracic vertebrae (HP:0008437) help
..expandCuboid-shaped vertebral bodies (HP:0004634) help
..expandDisc-like vertebral bodies (HP:0004591) help
..expandHemivertebrae (HP:0002937) help
..expandHypoplastic vertebral bodies (HP:0008479) help
..expandIncreased vertebral height (HP:0004570) help
..expandIrregularity of vertebral bodies (HP:0004582) help
..expandOvoid vertebral bodies (HP:0003300) help
..expandPatchy distortion of vertebrae (HP:0004609) help
..expandPear-shaped vertebrae (HP:0004566) help
..expandPlatyspondyly (HP:0000926) help
..expandSandwich appearance of vertebral bodies (HP:0004618) help
..expandVertebral arch anomaly (HP:0008438) help
..expandVertebral clefting (HP:0008428) help
..expandVertebral wedging (HP:0008422) 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:0005621HP:0005621Trapezoidal vertebral body0HHAT CL E G H5573318270OMIM:600092Nivelon-Nivelon-Mabille syndrome.


Genes (1) :HHAT

Diseases (1) :OMIM:600092
 

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