Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the neck (HP:0000464)help
Parent Node:
expandJoint stiffness (HP:0001387)help
Parent Node:
expandLimitation of neck motion (HP:0005986)help
..Starting node
..expandStiff neck (HP:0025258)help
Term ID: 25258
Name: Stiff neck
Synonym: Neck stiffness; Stiff neck
Definition: A sensation of tightness in the neck when attempting to move it, especially after a period of inactivity. Neck stiffness often involves soreness and difficulty moving the neck, especially when trying to turn the head to the side.
Comments:
Reference: HP:0025258
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLimited neck flexion (HP:0005991) help
..expandLimited neck range of motion (HP:0000466) help
..expandNeck joint contracture (HP:0005997) help
..expandNuchal rigidity (HP:0031179) 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:0025258HP:0025258Stiff neck0COL2A1 CL E G H12802200OMIM:616583Spondyloepiphyseal dysplasia, Stanescu type.284
HP:0025258HP:0025258Stiff neck0DKK1 CL E G H229432891ORPHA:268882Arnold-Chiari malformation type IHP:0040282 - Frequent
HP:0025258HP:0025258Stiff neck0NDE1 CL E G H5482017619ORPHA:2177HydranencephalyHP:0040282 - Frequent96
HP:0025258HP:0025258Stiff neck0NDUFS3 CL E G H47227710OMIM:618230Mitochondrial complex I deficiency, nuclear type 822
HP:0025258HP:0025258Stiff neck0NEK9 CL E G H9175418591OMIM:617022Lethal congenital contracture syndrome 10.9


Genes (5) :COL2A1 DKK1 NDE1 NDUFS3 NEK9

Diseases (5) :OMIM:616583 ORPHA:268882 ORPHA:2177 OMIM:618230 OMIM:617022
 

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