PSMNSW
MCID: PRS118
MIFTS: 12

Parasomnia, Sleepwalking Type (PSMNSW)

Aliases & Classifications for Parasomnia, Sleepwalking Type

MalaCards integrated aliases for Parasomnia, Sleepwalking Type:

Name: Parasomnia, Sleepwalking Type 56 13 71
Psmnsw 56

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant
multifactorial

Miscellaneous:
onset of sleepwalking between 4 and 8 years old
sleepwalking usually remits in adolescence
prevalence of sleepwalking up to 26% in childhood
prevalence of sleepwalking about 3% in adults
sleepwalking triggered by alcohol, sleep deprivation, stress
onset of sleep terrors between age 4 and 12 years old
sleep terrors usually remit during adolescence
prevalence of sleep terrors about 3% in children
prevalence of sleep terrors less than 1% in adults
affected individuals have amnesia for events


HPO:

31
parasomnia, sleepwalking type:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 56 613938
MedGen 41 C3151363
SNOMED-CT via HPO 68 263681008 89675003
UMLS 71 C3151363

Summaries for Parasomnia, Sleepwalking Type

OMIM : 56 Sleepwalking (SW) is a disorder in which a series of complex behaviors are initiated during slow-wave (non-REM) sleep and result in walking during sleep (American Academy of Sleep Medicine, 2005). It is a parasomnia, defined as a clinical disorder resulting in undesirable physical phenomena that occur predominantly during sleep. Parasomnias are not abnormalities of the processes responsible for sleep and wake states (summary by Hublin and Kaprio, 2003). Sleepwalking is more common in childhood (up to 26%), and usually resolves in adolescence; however, it can persist into adulthood (3%) (Hublin et al., 1997). (613938)

MalaCards based summary : Parasomnia, Sleepwalking Type, is also known as psmnsw. An important gene associated with Parasomnia, Sleepwalking Type is PSMNSW (Parasomnia, Sleepwalking Type). Related phenotype is sleep terror.

Related Diseases for Parasomnia, Sleepwalking Type

Symptoms & Phenotypes for Parasomnia, Sleepwalking Type

Human phenotypes related to Parasomnia, Sleepwalking Type:

31
# Description HPO Frequency HPO Source Accession
1 sleep terror 31 HP:0030765

Symptoms via clinical synopsis from OMIM:

56
Neurologic Central Nervous System:
walking during slow-wave sleep (sleepwalking)
sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors)

Clinical features from OMIM:

613938

Drugs & Therapeutics for Parasomnia, Sleepwalking Type

Search Clinical Trials , NIH Clinical Center for Parasomnia, Sleepwalking Type

Genetic Tests for Parasomnia, Sleepwalking Type

Anatomical Context for Parasomnia, Sleepwalking Type

Publications for Parasomnia, Sleepwalking Type

Articles related to Parasomnia, Sleepwalking Type:

# Title Authors PMID Year
1
Identification of sleepwalking gene(s): not yet, but soon? 56
21205687 2011
2
Novel genetic findings in an extended family pedigree with sleepwalking. 56
21205695 2011
3
Genetic aspects and genetic epidemiology of parasomnias. 56
14573377 2003
4
HLA and genetic susceptibility to sleepwalking. 56
12556916 2003
5
Prevalence and genetics of sleepwalking: a population-based twin study. 56
9008515 1997
6
Hereditary factors in sleepwalking and night terrors. 56
7426840 1980
7
Sleep-walking in twins. 56
4195120 1970
8
Atypical presentation of NREM arousal parasomnia with repetitive episodes. 61
17662022 2007

Variations for Parasomnia, Sleepwalking Type

Expression for Parasomnia, Sleepwalking Type

Search GEO for disease gene expression data for Parasomnia, Sleepwalking Type.

Pathways for Parasomnia, Sleepwalking Type

GO Terms for Parasomnia, Sleepwalking Type

Sources for Parasomnia, Sleepwalking Type

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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