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 spondylosis (HP:0008480)help
Term ID: 8480
Name: Cervical spondylosis
Synonym: Cervical osteoarthritis; Cervical spine degeneration; Neck arthritis
Definition: The presence of arthrosis, i.e., of degenerative joint disease, affecting the cervical vertebral column.
Comments:
Reference: HP:0008480
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 hypermobility (HP:0003318) help
..expandCervical spine instability (HP:0010646) 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:0008480HP:0008480Cervical spondylosis0HTRA1 CL E G H56549476ORPHA:199354Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy34


Genes (1) :HTRA1

Diseases (1) :ORPHA:199354
 

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