Human Phenotype Ontology 
Grandparent Node:
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Abnormality of central nervous system electrophysiology (HP:0030178)help
Grandparent Node:
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Abnormality of peripheral nervous system electrophysiology (HP:0030177)help
Parent Node:
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Abnormality of somatosensory evoked potentials (HP:0007377)help
..Starting node
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Prolonged somatosensory evoked potentials (HP:0007104)help
Term ID: 7104
Name: Prolonged somatosensory evoked potentials
Synonym:
Definition:
Comments:
Reference: HP:0007104
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of central somatosensory evoked potentials (HP:0100291) help
..expandAbnormality of peripheral somatosensory evoked potentials (HP:0100290) help
..expandEnhancement of the C-reflex (HP:0001340) help
..expandGiant somatosensory evoked potentials (HP:0001312) 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:0007104HP:0007104Prolonged somatosensory evoked potentials0TBC1D24 CL E G H5746529203OMIM:608105Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp.271
HP:0007104HP:0007104Prolonged somatosensory evoked potentials0TBC1D24 CL E G H5746529203ORPHA:163727Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndromeHP:0040282 - Frequent271


Genes (1) :TBC1D24

Diseases (2) :OMIM:608105 ORPHA:163727
 

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