Human Phenotype Ontology 
Grandparent Node:
expandInvoluntary movements (HP:0004305)help
Parent Node:
expandMyoclonus (HP:0001336)help
..Starting node
..expandErratic myoclonus (HP:0025357)help
Term ID: 25357
Name: Erratic myoclonus
Synonym: Fragmentary myoclonus
Definition: A type of myoclonus in which the myoclonias shift from body region to another in a random and asynchronous fashion. Erratic myoclonus can affect the face or limbs, are brief, single or repetitive, very frequent and nearly continuous.
Comments:
Reference: HP:0025357
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChin myoclonus (HP:0012462) help
..expandCortical myoclonus (HP:0040148) help
..expandEyelid myoclonus (HP:0025097) help
..expandLimb myoclonus (HP:0045084) help
..expandMorning myoclonic jerks (HP:0007000) help
..expandMyoclonic spasms (HP:0003739) help
..expandPalatal tremor (HP:0010530) help
..expandSleep myoclonus (HP:0012323) help
..expandSpinal myoclonus (HP:0010531) 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:0025357HP:0025357Erratic myoclonus0ARX CL E G H17030218060OMIM:308350Developmental and epileptic encephalopathy 1166
HP:0025357HP:0025357Erratic myoclonus0ATP6V0A1 CL E G H535865OMIM:6199711
HP:0025357HP:0025357Erratic myoclonus0EPM2A CL E G H79573413ORPHA:501Lafora diseaseHP:0040282 - Frequent83
HP:0025357HP:0025357Erratic myoclonus0KIF1C CL E G H107496317ORPHA:397946Autosomal spastic paraplegia type 58HP:0040282 - Frequent38
HP:0025357HP:0025357Erratic myoclonus0NHLRC1 CL E G H37888421576ORPHA:501Lafora diseaseHP:0040282 - Frequent77


Genes (5) :ARX ATP6V0A1 EPM2A KIF1C NHLRC1

Diseases (4) :OMIM:308350 OMIM:619971 ORPHA:501 ORPHA:397946
 

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