Human Phenotype Ontology 
Grandparent Node:
expandEMG abnormality (HP:0003457)help
Parent Node:
expandEMG: impaired neuromuscular transmission (HP:0100285)help
..Starting node
..expandEMG: incremental response of compound muscle action potential to repetitive nerve stimulation (HP:0030206)help
Term ID: 30206
Name: EMG: incremental response of compound muscle action potential to repetitive nerve stimulation
Synonym:
Definition: A compound muscle action potential (CMAP) is a type of electromyography (EMG). CMAP refers to a group of almost simultaneous action potentials from several muscle fibers in the same area evoked by stimulation of the supplying motor nerve and are recorded as one multipeaked summated action potential. This abnormality refers to an abnormal increase in the amplitude during the course of the investigation.
Comments:
Reference: HP:0030206
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEMG: decremental response of compound muscle action potential to repetitive nerve stimulation (HP:0003403) help
..expandIncreased jitter at single fiber EMG (HP:0030205) 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:0030206HP:0030206EMG: incremental response of compound muscle action potential to repetitive nerve stimulation0 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.