Sleep disturbance

Symptom Information:

Symptom ID: HPO:0002360
Synonyms:
Sleep disturbances [HPO:0002360]
Sleep dysfunction [HPO:0002360]
Sleep disorder [Orphanet:43440]
Sleep disorder (disorder) [Orphanet:43440]
Disturbance in sleep behavior (finding) [Orphanet:43440]
Dyssomnia (disorder) [Orphanet:43440]
Dyssomnias [Orphanet:43440]
Sleep disturbances [Orphanet:43440]
Sleep Disorders [Orphanet:43440]
Sleep disturbance [OMIM:Sleep disturbance]
Sleep disturbances [OMIM:Sleep disturbances]
Sleep and vigilance disorders [Orphanet:43440]
Dyssomnia [Orphanet:43440]
Unspecified sleep disturbance [Orphanet:43440]
Dyssomnia [MedDRA:10061827]
Dysfunctions associated with sleep stages or arousal from sleep [MedDRA:10061827]
Dyssomnia NOS [MedDRA:10061827]
Other dysfunctions of sleep stages or arousal from sleep [MedDRA:10061827]
Sleep disorder [MedDRA:10040984]
Aftersleeping [MedDRA:10040984]
Disorder sleep [MedDRA:10040984]
Nonorganic sleep disorder, unspecified [MedDRA:10040984]
Other sleep disturbances [MedDRA:10040984]
Other specific disorders of sleep of nonorganic origin [MedDRA:10040984]
Sleep disorder NOS [MedDRA:10040984]
Sleep disturbance [MedDRA:10040984]
Sleep disturbances [MedDRA:10040984]
Sleep disturbed [MedDRA:10040984]
Sleep problem [MedDRA:10040984]
Specific disorders of sleep [MedDRA:10040984]
Specific disorders of sleep of nonorganic origin [MedDRA:10040984]
Unspecified sleep disturbance [MedDRA:10040984]
Sleep disorder (NOS) [MedDRA:10040984]
Non-organic sleep disorder, unspecified [MedDRA:10040984]
Specific disorders of sleep of non-organic origin [MedDRA:10040984]
Change in sleep pattern [MedDRA:10040984]
Sleep disorder [OMIM:Sleep disorder]
Sleep disorders [OMIM:Sleep disorders]
Sleeping disturbances [OMIM:Sleeping disturbances]
Consciousness disorder [Orphanet:43440]
Consciousness Disorders [Orphanet:43440]
Sleep disturbances (incl subtypes) [MedDRA:10040998]
Dyssomnias [MedDRA:10013980]
Quality:
Cross references:
Orphanet:43440 "Sleep and vigilance disorders" [Orphanet:43440]
OMIM: "Sleep disturbance" [OMIM:Sleep disturbance]
OMIM: "Sleep disturbances" [OMIM:Sleep disturbances]
OMIM: "Sleep disorder" [OMIM:Sleep disorder]
OMIM: "Sleep disorders" [OMIM:Sleep disorders]
OMIM: "Sleeping disturbances" [OMIM:Sleeping disturbances]
UMLS:C0700201 "Dyssomnias" [Orphanet:43440]
UMLS:C0037317 "Sleep disturbances" [Orphanet:43440]
UMLS:C0851578 "Sleep Disorders" [Orphanet:43440]
UMLS:C0009792 "Consciousness Disorders" [Orphanet:43440]
Is a (Direct Parents):
MedDRA Sleep disorders NEC
HPO         Behavioral abnormality
HPO         Narcolepsy
MedDRA Nervous system disorders
MedDRA Sleep disturbances NEC
Orphanet Functional anomalies of the nervous system
MedDRA Sleep disorders and disturbances
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Behavioral abnormality(HPO:0000708)
                   Sleep disturbance(HPO:0002360)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Sleep disturbance(HPO:0002360)
Database Frequency: 113 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
1q21.1 microdeletion syndrome (Orphanet:250989)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
4q21 microdeletion syndrome (Orphanet:238750)
5p13 microduplication syndrome (Orphanet:329802)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Acromegaly (Orphanet:963)
Adiposis dolorosa (Orphanet:36397)
Alexander disease (Orphanet:58)
Alström syndrome (Orphanet:64)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Aspartylglucosaminuria (Orphanet:93)
Athyreosis (Orphanet:95713)
Atypical Rett syndrome (Orphanet:3095)
Atypical teratoid tumor (Orphanet:99966)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
Brain-lung-thyroid syndrome (Orphanet:209905)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
CK syndrome (Orphanet:251383)
CLN1 disease (Orphanet:228329)
CLN7 disease (Orphanet:228366)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Central congenital hypothyroidism (Orphanet:226298)
Central diabetes insipidus (Orphanet:178029)
Char syndrome (Orphanet:46627)
Choreoacanthocytosis (Orphanet:2388)
Christianson syndrome (Orphanet:85278)
Chronic hiccup (Orphanet:396)
Congenital hypothyroidism (Orphanet:442)
Congenital hypothyroidism due to developmental anomaly (Orphanet:95711)
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies (Orphanet:95715)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Encephalopathy due to GLUT1 deficiency (Orphanet:71277)
Familial advanced sleep-phase syndrome (Orphanet:164736)
Familial thyroid dyshormonogenesis (Orphanet:95716)
GILLES DE LA TOURETTE SYNDROME (OMIM:137580)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Hereditary hyperekplexia (Orphanet:3197)
Huntington disease (Orphanet:399)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypernychthemeral syndrome (Orphanet:73267)
Hypothyroidism due to TSH receptor mutations (Orphanet:90673)
Hypothyroidism due to deficient transcription factors involved in pituitary development or function (Orphanet:226307)
Idiopathic congenital hypothyroidism (Orphanet:95717)
Idiopathic hypersomnia (Orphanet:33208)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Infant botulism (Orphanet:178478)
Intellectual deficiency - hypotonia - spasticity - sleep disorder (Orphanet:356996)
Isolated thyroid-stimulating hormone deficiency (Orphanet:90674)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Leigh syndrome (Orphanet:506)
Lissencephaly due to LIS1 mutation (Orphanet:95232)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 (OMIM:616116)
Marfan syndrome (Orphanet:558)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Mild Canavan disease (Orphanet:314918)
Mucopolysaccharidosis type 3 (Orphanet:581)
Muscular pseudohypertrophy - hypothyroidism (Orphanet:2349)
Narcolepsy without cataplexy (Orphanet:83465)
Narcolepsy-cataplexy (Orphanet:2073)
Neuralgic amyotrophy (Orphanet:2901)
Niemann-Pick disease type C (Orphanet:646)
Norrie disease (Orphanet:649)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
PEHO syndrome (Orphanet:2836)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D (OMIM:613811)
Peripheral hypothyroidism (Orphanet:226310)
Peripheral resistance to thyroid hormones (Orphanet:97927)
Permanent congenital hypothyroidism (Orphanet:226292)
Perry syndrome (Orphanet:178509)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Porphyria (Orphanet:738)
Prader-Willi syndrome (Orphanet:739)
Primary congenital hypothyroidism (Orphanet:226295)
Primary congenital hypothyroidism without thyroid developmental anomaly (Orphanet:95714)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
Resistance to thyrotropin-releasing hormone syndrome (Orphanet:99832)
Rett syndrome (Orphanet:778)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Scheie syndrome (Orphanet:93474)
Septo-optic dysplasia (Orphanet:3157)
Severe Canavan disease (Orphanet:314911)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Spontaneous periodic hypothermia (Orphanet:29822)
Thyroid ectopia (Orphanet:95712)
Thyroid hemiagenesis (Orphanet:95719)
Transient congenital hypothyroidism (Orphanet:178045)
Vici syndrome (Orphanet:1493)
Whipple disease (Orphanet:3452)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolfram-like syndrome (ORPHA:411590)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)
X-linked Charcot-Marie-Tooth disease type 2 (Orphanet:101076)
X-linked Charcot-Marie-Tooth disease type 3 (Orphanet:101077)
X-linked Charcot-Marie-Tooth disease type 4 (Orphanet:101078)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)
Young adult-onset Parkinsonism (Orphanet:2828)