Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebellum morphology (HP:0001317)help
Grandparent Node:
expandAbnormality of coordination (HP:0011443)help
Parent Node:
expandAtaxia (HP:0001251)help
..Starting node
..expandDyssynergia (HP:0010867)help
Term ID: 10867
Name: Dyssynergia
Synonym:
Definition: A type of ataxia characterized by the impairment of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed. With dyssynergia, a voluntary movement appears broken down into its component parts.
Comments:
Reference: HP:0010867
Genes and Diseases:
 
       Child Nodes:
........expandOcular dyssynergia (HP:0010868) help
........expandAsynergia (HP:0010869) help

 Sister Nodes: 
..expandCerebellar ataxia associated with quadrupedal gait (HP:0009878) help
..expandDysdiadochokinesis (HP:0002075) help
..expandDysmetria (HP:0001310) help
..expandEpisodic ataxia (HP:0002131) help
..expandGait ataxia (HP:0002066) help
..expandLimb ataxia (HP:0002070) help
..expandNonprogressive cerebellar ataxia (HP:0002470) help
..expandProgressive cerebellar ataxia (HP:0002073) help
..expandSpastic ataxia (HP:0002497) help
..expandTruncal ataxia (HP:0002078) 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:0010867HP:0010867Dyssynergia0ATN1 CL E G H18223033ORPHA:101Dentatorubral pallidoluysian atrophyHP:0040282 - Frequent16
HP:0010867HP:0010869Asynergia1 CL E G H
HP:0010867HP:0010868Ocular dyssynergia1 CL E G H


Genes (1) :ATN1

Diseases (1) :ORPHA:101
 

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