Human Phenotype Ontology 
Grandparent Node:
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Behavioral abnormality (HP:0000708)help
Parent Node:
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Sleep disturbance (HP:0002360)help
..Starting node
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Parasomnia (HP:0025234)help
Term ID: 25234
Name: Parasomnia
Synonym:
Definition: An undesirable physical event or experience that occurs during entry into sleep, during sleep, or during arousal from sleep.
Comments:
Reference: HP:0025234
Genes and Diseases:
 
       Child Nodes:
........expandNon-rapid eye movement parasomnia (HP:0025235) help
................... HP:0025236 Somnambulism
................... HP:0025237 Confusional arousal
................... HP:0030765 Sleep terror

 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
..expandRestless legs (HP:0012452) help
..expandSleep apnea (HP:0010535) help
..expandSleep paralysis (HP:0025233) 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:0025234HP:0025234Parasomnia0CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy94
HP:0025234HP:0025234Parasomnia0CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy188
HP:0025234HP:0025234Parasomnia0CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy225
HP:0025234HP:0025234Parasomnia0CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy88
HP:0025234HP:0025234Parasomnia0CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy1
HP:0025234HP:0025234Parasomnia0DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy172
HP:0025234HP:0025234Parasomnia0KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy321
HP:0025234HP:0025234Parasomnia0MAGEL2 CL E G H545516814ORPHA:398069MAGEL2-related Prader-Willi-like syndrome63
HP:0025234HP:0025234Parasomnia0SIM1 CL E G H649210882ORPHA:398079SIM1-related Prader-Willi-like syndrome40
HP:0025234HP:0025234Parasomnia0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type II82
HP:0025234HP:0025234Parasomnia0SMO CL E G H660811119OMIM:241800Hypothalamic hamartomascongenital hypothalamic hamartoma syndrome, included22
HP:0025234HP:0025234Parasomnia0TFAP2B CL E G H702111743OMIM:169100Char syndrome.104
HP:0025234HP:0025235Non-rapid eye movement parasomnia1CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare94
HP:0025234HP:0025235Non-rapid eye movement parasomnia1CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare188
HP:0025234HP:0025235Non-rapid eye movement parasomnia1CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare225
HP:0025234HP:0025235Non-rapid eye movement parasomnia1CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare88
HP:0025234HP:0025235Non-rapid eye movement parasomnia1CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare1
HP:0025234HP:0025235Non-rapid eye movement parasomnia1DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare172
HP:0025234HP:0025235Non-rapid eye movement parasomnia1KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare321
HP:0025234HP:0025235Non-rapid eye movement parasomnia1MAGEL2 CL E G H545516814ORPHA:398069MAGEL2-related Prader-Willi-like syndrome63
HP:0025234HP:0025235Non-rapid eye movement parasomnia1SIM1 CL E G H649210882ORPHA:398079SIM1-related Prader-Willi-like syndrome40
HP:0025234HP:0025235Non-rapid eye movement parasomnia1SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type II82
HP:0025234HP:0025235Non-rapid eye movement parasomnia1SMO CL E G H660811119OMIM:241800Hypothalamic hamartomascongenital hypothalamic hamartoma syndrome, included22
HP:0025234HP:0025237Confusional arousal2CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional94
HP:0025234HP:0025236Somnambulism2CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional94
HP:0025234HP:0025237Confusional arousal2CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional188
HP:0025234HP:0025236Somnambulism2CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional188
HP:0025234HP:0025236Somnambulism2CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional225
HP:0025234HP:0025237Confusional arousal2CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional225
HP:0025234HP:0025237Confusional arousal2CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional88
HP:0025234HP:0025236Somnambulism2CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional88
HP:0025234HP:0025237Confusional arousal2CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional1
HP:0025234HP:0025236Somnambulism2CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional1
HP:0025234HP:0025237Confusional arousal2DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional172
HP:0025234HP:0025236Somnambulism2DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional172
HP:0025234HP:0025237Confusional arousal2KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional321
HP:0025234HP:0025236Somnambulism2KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040283 - Occasional321
HP:0025234HP:0025237Confusional arousal2MAGEL2 CL E G H545516814ORPHA:398069MAGEL2-related Prader-Willi-like syndromeHP:0040283 - Occasional63
HP:0025234HP:0025237Confusional arousal2SIM1 CL E G H649210882ORPHA:398079SIM1-related Prader-Willi-like syndromeHP:0040283 - Occasional40
HP:0025234HP:0030765Sleep terror2SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040282 - Frequent82
HP:0025234HP:0030765Sleep terror2SMO CL E G H660811119OMIM:241800Hypothalamic hamartomascongenital hypothalamic hamartoma syndrome, included22


Genes (12) :CABP4 CHRNA2 CHRNA4 CHRNB2 CRH DEPDC5 KCNT1 MAGEL2 SIM1 SLC25A13 SMO TFAP2B

Diseases (6) :ORPHA:98784 ORPHA:398069 ORPHA:398079 ORPHA:247585 OMIM:241800 OMIM:169100
 

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