Human Phenotype Ontology 
Grandparent Node:
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Abnormality of central nervous system electrophysiology (HP:0030178)help
Parent Node:
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Abnormal motor evoked potentials (HP:0012896)help
..Starting node
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Abnormal lower-limb motor evoked potentials (HP:0012898)help
Term ID: 12898
Name: Abnormal lower-limb motor evoked potentials
Synonym: Abnormal motor evoked potentials in the lower limb
Definition: An anomaly identified by motor evoked potentials (MEPs) in the leg.
Comments:
Reference: HP:0012898
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal upper-limb motor evoked potentials (HP:0012897) 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:0012898HP:0012898Abnormal lower-limb motor evoked potentials0CPT1C CL E G H12612918540ORPHA:444099Autosomal dominant spastic paraplegia type 73HP:0040282 - Frequent1


Genes (1) :CPT1C

Diseases (1) :ORPHA:444099
 

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