Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the vertebral column (HP:0000925)help
Parent Node:
expandAbnormal vertebral morphology (HP:0003468)help
..Starting node
..expandDysplasia of second lumbar vertebra (HP:0004589)help
Term ID: 4589
Name: Dysplasia of second lumbar vertebra
Synonym:
Definition:
Comments:
Reference: HP:0004589
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal form of the vertebral bodies (HP:0003312) help
..expandAbnormal number of vertebrae (HP:0030304) help
..expandAbnormality of vertebral epiphysis morphology (HP:0100734) help
..expandAbnormally ossified vertebrae (HP:0100569) help
..expandAplasia/Hypoplasia of the vertebrae (HP:0008515) help
..expandModic type vertebral endplate changes (HP:0030775) help
..expandMorbus Scheuermann (HP:0010891) help
..expandMultiple small vertebral fractures (HP:0005877) help
..expandOsteoporosis of vertebrae (HP:0005625) help
..expandPunctate vertebral calcifications (HP:0008420) help
..expandSchmorl's node (HP:0030041) help
..expandSclerotic vertebral body (HP:0100861) help
..expandVertebral compression fracture (HP:0002953) help
..expandVertebral hyperostosis (HP:0008442) help
..expandVertebral segmentation defect (HP:0003422) 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:0004589HP:0004589Dysplasia of second lumbar vertebra0 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.