Human Phenotype Ontology 
Grandparent Node:
expandVertebral fusion (HP:0002948)help
Parent Node:
expandFused cervical vertebrae (HP:0002949)help
..Starting node
..expandCervical C3/C4 vertebral fusion (HP:0030281)help
Term ID: 30281
Name: Cervical C3/C4 vertebral fusion
Synonym:
Definition: Fusion of cervical vertebrae at C3 and C4, caused by a failure in the normal segmentation or division of the cervical vertebrae during the early weeks of fetal development.
Comments:
Reference: HP:0030281
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCervical C2/C3 vertebral fusion (HP:0004602) help
..expandCervical C5/C6 vertebrae fusion (HP:0004635) help
..expandFusion of midcervical facet joints (HP:0004575) help
..expandProgressive cervical vertebral spine fusion (HP:0008449) 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:0030281HP:0030281Cervical C3/C4 vertebral fusion0GDF3 CL E G H95734218OMIM:613702Klippel-Feil syndrome 3, autosomal dominant7


Genes (1) :GDF3

Diseases (1) :OMIM:613702
 

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