Human Phenotype Ontology 
Grandparent Node:
expandBehavioral abnormality (HP:0000708)help
Parent Node:
expandSleep disturbance (HP:0002360)help
..Starting node
..expandSleep paralysis (HP:0025233)help
Term ID: 25233
Name: Sleep paralysis
Synonym:
Definition: An inability to move the body at sleep onset or upon awakening from sleep lasting seconds to a few minutes.
Comments:
Reference: HP:0025233
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal rapid eye movement sleep (HP:0002494) help
..expandBruxism (HP:0003763) help
..expandExcessive daytime somnolence (HP:0001262) help
..expandHypersomnia (HP:0100786) help
..expandInsomnia (HP:0100785) help
..expandNarcolepsy (HP:0030050) help
..expandobsolete Excessive daytime sleepiness (HP:0002189) help
..expandParasomnia (HP:0025234) help
..expandRestless legs (HP:0012452) help
..expandSleep apnea (HP:0010535) help
..expandSleep-wake cycle disturbance (HP:0006979) help
..expandSnoring (HP:0025267) 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:0025233HP:0025233Sleep paralysis0HCRT CL E G H30604847OMIM:161400Narcolepsy 11


Genes (1) :HCRT

Diseases (1) :OMIM:161400
 

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