Human Phenotype Ontology 
Grandparent Node:
expandAbnormal axial skeleton morphology (HP:0009121)help
Parent Node:
expandAbnormality of the vertebral column (HP:0000925)help
..Starting node
..expandSpinal dysplasia (HP:0008423)help
Term ID: 8423
Name: Spinal dysplasia
Synonym:
Definition: The presence of developmental dysplasia of the vertebral column.
Comments:
Reference: HP:0008423
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal coccyx morphology (HP:0008519) help
..expandAbnormal intervertebral disk morphology (HP:0005108) help
..expandAbnormal lumbar spine morphology (HP:0100712) help
..expandAbnormal sacrum morphology (HP:0005107) help
..expandAbnormal thoracic spine morphology (HP:0100711) help
..expandAbnormal vertebral morphology (HP:0003468) help
..expandAbnormality of the cervical spine (HP:0003319) help
..expandAbnormality of the curvature of the vertebral column (HP:0010674) help
..expandAbnormality of the odontoid process (HP:0003310) help
..expandAplasia/Hypoplasia involving the vertebral column (HP:0008518) help
..expandAtlantoaxial abnormality (HP:0003413) help
..expandBack pain (HP:0003418) help
..expandNeuropathic spinal arthropathy (HP:0008443) help
..expandReversed usual vertebral column curves (HP:0008433) help
..expandSpinal canal stenosis (HP:0003416) help
..expandSpinal instability (HP:0005881) help
..expandSpinal rigidity (HP:0003306) help
..expandSpondylolisthesis (HP:0003302) help
..expandSpondylolysis (HP:0003304) 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:0008423HP:0008423Spinal dysplasia0 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.