Human Phenotype Ontology 
Grandparent Node:
expandAtaxia (HP:0001251)help
Parent Node:
expandDyssynergia (HP:0010867)help
..Starting node
..expandAsynergia (HP:0010869)help
Term ID: 10869
Name: Asynergia
Synonym:
Definition: A type of dyssynergy characterized by the lack of the ability to smoothly perform the elements of a voluntary movement in the appropriate order and speed.
Comments:
Reference: HP:0010869
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandOcular dyssynergia (HP:0010868) 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:0010869HP:0010869Asynergia0 CL E G H


Genes (0) :

Diseases (0) :
 

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