Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the vertebral column (HP:0000925)help
Parent Node:
expandAbnormality of the cervical spine (HP:0003319)help
..Starting node
..expandCervical spine hypermobility (HP:0003318)help
Term ID: 3318
Name: Cervical spine hypermobility
Synonym: Cervical spine joint hypermobility
Definition:
Comments:
Reference: HP:0003318
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal cervical curvature (HP:0005905) help
..expandAplasia/Hypoplasia of the cervical spine (HP:0011041) help
..expandC1-C2 vertebral abnormality (HP:0008440) help
..expandCervical platyspondyly (HP:0004558) help
..expandCervical spine instability (HP:0010646) help
..expandCervical spondylosis (HP:0008480) help
..expandCervical subluxation (HP:0003308) help
..expandCervical vertebral bodies with decreased anteroposterior diameter (HP:0008483) help
..expandCervical vertebral dysplasia (HP:0008469) help
..expandDecreased cervical spine mobility (HP:0004637) help
..expandEnlarged sagittal diameter of the cervical canal (HP:0005878) help
..expandShort neck (HP:0000470) help
..expandWidening of cervical spinal canal (HP:0004571) 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:0003318HP:0003318Cervical spine hypermobility0FGD1 CL E G H22453663OMIM:305400Aarskog-Scott syndrome.62


Genes (1) :FGD1

Diseases (1) :OMIM:305400
 

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