Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vertebral morphology (HP:0003468)help
Parent Node:
expandAbnormal form of the vertebral bodies (HP:0003312)help
..Starting node
..expandAbnormality of the vertebral spinous processes (HP:0008516)help
Term ID: 8516
Name: Abnormality of the vertebral spinous processes
Synonym:
Definition:
Comments:
Reference: HP:0008516
Genes and Diseases:
 
       Child Nodes:
........expandAbsent spinous processes of lower thoracic and lumbar vertebrae (HP:0008464) help

 Sister Nodes: 
..expandAbnormality of spinal facet joint (HP:0030870) help
..expandAbnormality of the vertebral endplates (HP:0005106) 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
..expandTrapezoidal vertebral body (HP:0005621) 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:0008516HP:0008516Abnormality of the vertebral spinous processes0CDH11 CL E G H10091750ORPHA:1299Branchioskeletogenital syndromeHP:0040281 - Very frequent2
HP:0008516HP:0008516Abnormality of the vertebral spinous processes0CYP27A1 CL E G H15932605ORPHA:909Cerebrotendinous xanthomatosisHP:0040283 - Occasional114
HP:0008516HP:0008464Absent spinous processes of lower thoracic and lumbar vertebrae1 CL E G H


Genes (2) :CDH11 CYP27A1

Diseases (2) :ORPHA:1299 ORPHA:909
 

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