以 HPO 交叉檢視

HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。

搜尋 HPO

Sleep disturbance

HP:0002360

對應病歷用詞(0)

尚無對應用詞。

具此 HPO 的疾病（附加參考）(172)

African trypanosomiasisORPHA:3385 · Very frequent (99-80%)
Alexander diseaseORPHA:58 · Very frequent (99-80%)
Angelman syndromeORPHA:72 · Very frequent (99-80%)
Atypical Rett syndromeORPHA:3095 · Very frequent (99-80%)
Brain dopamine-serotonin vesicular transport diseaseORPHA:352649 · Very frequent (99-80%)
CK syndromeORPHA:251383 · Very frequent (99-80%)
Encephalitis lethargicaORPHA:83600 · Very frequent (99-80%)
Familial Alzheimer-like prion diseaseORPHA:280397 · Very frequent (99-80%)
Hypermobile Ehlers-Danlos syndromeORPHA:285 · Very frequent (99-80%)
Idiopathic hypersomniaORPHA:33208 · Very frequent (99-80%)
Infant botulismORPHA:178478 · Very frequent (99-80%)
Intellectual disability-epilepsy-extrapyramidal syndromeORPHA:468620 · Very frequent (99-80%)
Mucopolysaccharidosis type 3ORPHA:581 · Very frequent (99-80%)
Muscular pseudohypertrophy-hypothyroidism syndromeORPHA:2349 · Very frequent (99-80%)
Narcolepsy type 1ORPHA:2073 · Very frequent (99-80%)
Narcolepsy type 2ORPHA:83465 · Very frequent (99-80%)
Opsoclonus-myoclonus syndromeORPHA:1183 · Very frequent (99-80%)
Perry syndromeORPHA:178509 · Very frequent (99-80%)
Pitt-Hopkins syndromeORPHA:2896 · Very frequent (99-80%)
Pontocerebellar hypoplasia type 2ORPHA:2524 · Very frequent (99-80%)
Progeria-short stature-pigmented nevi syndromeORPHA:2959 · Very frequent (99-80%)
Smith-Magenis syndromeORPHA:819 · Very frequent (99-80%)
X-linked intellectual disability-psychosis-macroorchidism syndromeORPHA:3077 · Very frequent (99-80%)
17q11 microdeletion syndromeORPHA:97685 · Frequent (79-30%)
2q23.1 microdeletion syndromeORPHA:228402 · Frequent (79-30%)
2q23.1 microduplication syndromeORPHA:313947 · Frequent (79-30%)
Allan-Herndon-Dudley syndromeORPHA:59 · Frequent (79-30%)
ANK3-related intellectual disability-sleep disturbance syndromeORPHA:356996 · Frequent (79-30%)
Aromatic L-amino acid decarboxylase deficiencyORPHA:35708 · Frequent (79-30%)
Autosomal dominant dopa-responsive dystoniaORPHA:98808 · Frequent (79-30%)
Beta-propeller protein-associated neurodegenerationORPHA:329284 · Frequent (79-30%)
Bohring-Opitz syndromeORPHA:97297 · Frequent (79-30%)
Bronchopulmonary dysplasiaORPHA:70589 · Frequent (79-30%)
Caribbean parkinsonismORPHA:97355 · Frequent (79-30%)
Chronic hiccupORPHA:396 · Frequent (79-30%)
Citrullinemia type IIORPHA:247585 · Frequent (79-30%)
Cornelia de Lange syndromeORPHA:199 · Frequent (79-30%)
CraniopharyngiomaORPHA:54595 · Frequent (79-30%)
Dopa-responsive dystonia due to sepiapterin reductase deficiencyORPHA:70594 · Frequent (79-30%)
Dopamine beta-hydroxylase deficiencyORPHA:230 · Frequent (79-30%)
Early infantile developmental and epileptic encephalopathyORPHA:1934 · Frequent (79-30%)
Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletionORPHA:284169 · Frequent (79-30%)
Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutationORPHA:466950 · Frequent (79-30%)
Familial gestational hyperthyroidismORPHA:99819 · Frequent (79-30%)
Familial hyperthyroidism due to mutations in TSH receptorORPHA:424 · Frequent (79-30%)
Familial Mediterranean feverORPHA:342 · Frequent (79-30%)
FOXG1 syndromeORPHA:561854 · Frequent (79-30%)
Fragile X syndromeORPHA:908 · Frequent (79-30%)
Gerstmann-Straussler-Scheinker syndromeORPHA:356 · Frequent (79-30%)
Hereditary hyperekplexiaORPHA:3197 · Frequent (79-30%)
HIDEA syndromeORPHA:436141 · Frequent (79-30%)
High altitude pulmonary edemaORPHA:330012 · Frequent (79-30%)
Hurler syndromeORPHA:93473 · Frequent (79-30%)
Hyperprolinemia type 2ORPHA:79101 · Frequent (79-30%)
HypophosphatasiaORPHA:436 · Frequent (79-30%)
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndromeORPHA:522077 · Frequent (79-30%)
Kleefstra syndromeORPHA:261494 · Frequent (79-30%)
Leukocyte adhesion deficiency type IIORPHA:99843 · Frequent (79-30%)
Marfan syndromeORPHA:558 · Frequent (79-30%)
Mowat-Wilson syndromeORPHA:2152 · Frequent (79-30%)
Mowat-Wilson syndrome due to a ZEB2 point mutationORPHA:261552 · Frequent (79-30%)
Mowat-Wilson syndrome due to monosomy 2q22ORPHA:261537 · Frequent (79-30%)
Mucopolysaccharidosis type 2ORPHA:580 · Frequent (79-30%)
MYT1L-related developmental delay-intellectual disability-obesity syndromeORPHA:647799 · Frequent (79-30%)
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiencyORPHA:88639 · Frequent (79-30%)
PANDASORPHA:66624 · Frequent (79-30%)
Parkinsonian-pyramidal syndromeORPHA:171695 · Frequent (79-30%)
Phelan-McDermid syndromeORPHA:48652 · Frequent (79-30%)
PMP22-RAI1 contiguous gene duplication syndromeORPHA:477817 · Frequent (79-30%)
Prader-Willi syndrome due to paternal 15q11q13 deletionORPHA:98793 · Frequent (79-30%)
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1ORPHA:177901 · Frequent (79-30%)
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2ORPHA:177904 · Frequent (79-30%)
Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndromeORPHA:363400 · Frequent (79-30%)
SATB2-associated syndrome due to a pathogenic variantORPHA:576283 · Frequent (79-30%)
Severe Canavan diseaseORPHA:314911 · Frequent (79-30%)
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndromeORPHA:391307 · Frequent (79-30%)
Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataractORPHA:500545 · Frequent (79-30%)
Silver-Russell syndromeORPHA:813 · Frequent (79-30%)
Smith-Lemli-Opitz syndromeORPHA:818 · Frequent (79-30%)
Spontaneous periodic hypothermiaORPHA:29822 · Frequent (79-30%)
Subacute sclerosing leukoencephalitisORPHA:2806 · Frequent (79-30%)
SYNGAP1-related developmental and epileptic encephalopathyORPHA:544254 · Frequent (79-30%)
Tuberous sclerosis complexORPHA:805 · Frequent (79-30%)
Uremic pruritusORPHA:94059 · Frequent (79-30%)
Usher syndrome type 2ORPHA:231178 · Frequent (79-30%)
Visual snow syndromeORPHA:420556 · Frequent (79-30%)
WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndromeORPHA:466943 · Frequent (79-30%)
Whipple diseaseORPHA:3452 · Frequent (79-30%)
White-Sutton syndromeORPHA:468678 · Frequent (79-30%)
Wolf-Hirschhorn syndromeORPHA:280 · Frequent (79-30%)
X-linked alpha-thalassemia-intellectual disability syndromeORPHA:847 · Frequent (79-30%)
X-linked intellectual disability, Najm typeORPHA:163937 · Frequent (79-30%)
Xq25 microduplication syndromeORPHA:521258 · Frequent (79-30%)
14q11.2 microduplication syndromeORPHA:261229 · Occasional (29-5%)
16p11.2p12.2 microdeletion syndromeORPHA:261211 · Occasional (29-5%)
1q21.1 microdeletion syndromeORPHA:250989 · Occasional (29-5%)
2q32q33 deletion syndromeORPHA:251019 · Occasional (29-5%)
2q37 microdeletion syndromeORPHA:1001 · Occasional (29-5%)
4q21 microdeletion syndromeORPHA:238750 · Occasional (29-5%)
7q11.23 microduplication syndromeORPHA:96121 · Occasional (29-5%)
Adiposis dolorosaORPHA:36397 · Occasional (29-5%)
Alazami syndromeORPHA:319671 · Occasional (29-5%)
Alexander disease type IIORPHA:363722 · Occasional (29-5%)
Amyotrophic lateral sclerosisORPHA:803 · Occasional (29-5%)
AspartylglucosaminuriaORPHA:93 · Occasional (29-5%)
Autosomal recessive spastic paraplegia type 20ORPHA:101000 · Occasional (29-5%)
Bainbridge-Ropers syndromeORPHA:352577 · Occasional (29-5%)
Bilateral generalized polymicrogyriaORPHA:208447 · Occasional (29-5%)
Burning mouth syndromeORPHA:353253 · Occasional (29-5%)
Char syndromeORPHA:46627 · Occasional (29-5%)
Christianson syndromeORPHA:85278 · Occasional (29-5%)
Classic glucose transporter type 1 deficiency syndromeORPHA:71277 · Occasional (29-5%)
Cockayne syndrome type 1ORPHA:90321 · Occasional (29-5%)
Congenital fiber-type disproportion myopathyORPHA:2020 · Occasional (29-5%)
Congenital infiltrating lipomatosis of the faceORPHA:583097 · Occasional (29-5%)
Congenital-onset Steinert myotonic dystrophyORPHA:589821 · Occasional (29-5%)
Contractures-developmental delay-Pierre Robin syndromeORPHA:436003 · Occasional (29-5%)
CTCF-related neurodevelopmental disorderORPHA:363611 · Occasional (29-5%)
Distal deletion 10q syndromeORPHA:96148 · Occasional (29-5%)
Dubowitz syndromeORPHA:235 · Occasional (29-5%)
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletionORPHA:268261 · Occasional (29-5%)
Fatal infantile lactic acidosis with methylmalonic aciduriaORPHA:17 · Occasional (29-5%)
Folinic acid-responsive seizuresORPHA:79097 · Occasional (29-5%)
Glycogen storage disease due to liver glycogen phosphorylase deficiencyORPHA:369 · Occasional (29-5%)
Glycogen storage disease due to liver phosphorylase kinase deficiencyORPHA:264580 · Occasional (29-5%)
Hao-Fountain syndrome due to 16p13.2 microdeletionORPHA:500055 · Occasional (29-5%)
Helsmoortel-Van der Aa syndromeORPHA:404448 · Occasional (29-5%)
Hereditary late-onset Parkinson diseaseORPHA:411602 · Occasional (29-5%)
Hyperphenylalaninemia due to tetrahydrobiopterin deficiencyORPHA:238583 · Occasional (29-5%)
Hypotonia-speech impairment-severe cognitive delay syndromeORPHA:371364 · Occasional (29-5%)
Idiopathic intracranial hypertensionORPHA:238624 · Occasional (29-5%)
Infantile neurovisceral acid sphingomyelinase deficiencyORPHA:77292 · Occasional (29-5%)
Intellectual disability-cardiac anomalies-short stature-joint laxity syndromeORPHA:508498 · Occasional (29-5%)
Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndromeORPHA:404473 · Occasional (29-5%)
Kleefstra syndrome due to 9q34 microdeletionORPHA:96147 · Occasional (29-5%)
Lafora diseaseORPHA:501 · Occasional (29-5%)
Landau-Kleffner syndromeORPHA:98818 · Occasional (29-5%)
Machado-Joseph disease type 1ORPHA:276238 · Occasional (29-5%)
Machado-Joseph disease type 2ORPHA:276241 · Occasional (29-5%)
Machado-Joseph disease type 3ORPHA:276244 · Occasional (29-5%)
Microcephalic cortical malformations-short stature due to RTTN deficiencyORPHA:468631 · Occasional (29-5%)
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndromeORPHA:476126 · Occasional (29-5%)
Neuralgic amyotrophyORPHA:2901 · Occasional (29-5%)
Niemann-Pick disease type CORPHA:646 · Occasional (29-5%)
Norrie diseaseORPHA:649 · Occasional (29-5%)
Ocular anomalies-axonal neuropathy-developmental delay syndromeORPHA:496790 · Occasional (29-5%)
PellagraORPHA:97352 · Occasional (29-5%)
PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndromeORPHA:589905 · Occasional (29-5%)
Postpoliomyelitis syndromeORPHA:2942 · Occasional (29-5%)
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15ORPHA:98754 · Occasional (29-5%)
Primary biliary cholangitisORPHA:186 · Occasional (29-5%)
Proximal myotonic myopathyORPHA:606 · Occasional (29-5%)
Q feverORPHA:781 · Occasional (29-5%)
Rett syndromeORPHA:778 · Occasional (29-5%)
Ring chromosome 15 syndromeORPHA:96177 · Occasional (29-5%)
SarcosinemiaORPHA:3129 · Occasional (29-5%)
Septo-optic dysplasia spectrumORPHA:3157 · Occasional (29-5%)
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndromeORPHA:363686 · Occasional (29-5%)
Spinocerebellar ataxia type 10ORPHA:98761 · Occasional (29-5%)
Sporadic Creutzfeldt-Jakob diseaseORPHA:204 · Occasional (29-5%)
Sturge-Weber syndromeORPHA:3205 · Occasional (29-5%)
Tick-borne encephalitisORPHA:297 · Occasional (29-5%)
Vici syndromeORPHA:1493 · Occasional (29-5%)
Wolfram syndromeORPHA:3463 · Occasional (29-5%)
X-linked Charcot-Marie-Tooth disease type 4ORPHA:101078 · Occasional (29-5%)
X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
X-linked intellectual disability due to GRIA3 mutationsORPHA:364028 · Occasional (29-5%)
Airway infantile hemangiomaORPHA:137935 · Very rare (<4-1%)
Alström syndromeORPHA:64 · Very rare (<4-1%)
Brain-lung-thyroid syndromeORPHA:209905 · Very rare (<4-1%)
ChoreoacanthocytosisORPHA:2388 · Very rare (<4-1%)
PreeclampsiaORPHA:275555 · Very rare (<4-1%)