Human Phenotype Ontology 
Grandparent Node:
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Abnormal form of the vertebral bodies (HP:0003312)help
Grandparent Node:
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Vertebral segmentation defect (HP:0003422)help
Parent Node:
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Hemivertebrae (HP:0002937)help
..Starting node
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Thoracic hemivertebrae (HP:0008467)help
Term ID: 8467
Name: Thoracic hemivertebrae
Synonym: Midthoracic hemivertebrae
Definition: Absence of one half of the vertebral body in the thoracic spine.
Comments:
Reference: HP:0008467
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCervical hemivertebrae (HP:0025481) help
..expandLumbar hemivertebrae (HP:0008439) 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:0008467HP:0008467Thoracic hemivertebrae0H3-3B CL E G H30214765OMIM:619721BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 2; BRYLIB2
HP:0008467HP:0008467Thoracic hemivertebrae0PUF60 CL E G H2282717042ORPHA:508498Intellectual disability-cardiac anomalies-short stature-joint laxity syndromeHP:0040283 - Occasional19
HP:0008467HP:0008467Thoracic hemivertebrae0ROR2 CL E G H492010257OMIM:268310Robinow syndrome, autosomal recessive.120
HP:0008467HP:0008467Thoracic hemivertebrae0STAG2 CL E G H1073511355OMIM:301043HOLOPROSENCEPHALY 13, X-LINKED; HPE131


Genes (4) :H3-3B PUF60 ROR2 STAG2

Diseases (4) :OMIM:619721 ORPHA:508498 OMIM:268310 OMIM:301043
 

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