Sleep disturbance
Symptom Information:
Symptom ID: | HPO:0002360 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |