Tremor

Symptom Information:

Symptom ID: HPO:0001337
Synonyms:
Tremor (finding) [Orphanet:43240]
Tremor [Orphanet:43240]
Tremor [OMIM:Tremor]
Tremor [MedDRA:10044565]
Essential and other specified forms of tremor [MedDRA:10044565]
Parkinsonian-like tremor [MedDRA:10044565]
Shakiness [MedDRA:10044565]
Shaking [MedDRA:10044565]
Shaking of hands [MedDRA:10044565]
Tongue tremor [MedDRA:10044565]
Tremble [MedDRA:10044565]
Trembling [MedDRA:10044565]
Tremor coarse [MedDRA:10044565]
Tremor fine [MedDRA:10044565]
Tremor finger [MedDRA:10044565]
Tremor limb [MedDRA:10044565]
Tremor muscle [MedDRA:10044565]
Tremor NEC [MedDRA:10044565]
Tremor nerve [MedDRA:10044565]
Tremor of hands [MedDRA:10044565]
Tremor perioral [MedDRA:10044565]
Tremor semirrhythmic [MedDRA:10044565]
Tremulousness [MedDRA:10044565]
Tremor aggravated [MedDRA:10044565]
Coarse tremor [OMIM:Coarse tremor]
Fine tremor [OMIM:Fine tremor]
Tremor (1 patient) [OMIM:Tremor (1 patient)]
Tremor (3 patients) [OMIM:Tremor (3 patients)]
Tremor (30%) [OMIM:Tremor (30%)]
Tremor (57% of patients) [OMIM:Tremor (57% of patients)]
Tremor (in some patients) [OMIM:Tremor (in some patients)]
Tremor (later-onset) [OMIM:Tremor (later-onset)]
Tremor (less common) [OMIM:Tremor (less common)]
Tremor (rare) [OMIM:Tremor (rare)]
Tremor, fine [OMIM:Tremor, fine]
Tremors [OMIM:Tremors]
Tremors (in hands) [OMIM:Tremors (in hands)]
Tremor (excl congenital) [MedDRA:10044566]
Tremor, mild, transient [OMIM,du]
Quality:
Cross references:
Orphanet:43240 "Tremor" [Orphanet:43240]
OMIM: "Tremor" [OMIM:Tremor]
OMIM: "Coarse tremor" [OMIM:Coarse tremor]
OMIM: "Fine tremor" [OMIM:Fine tremor]
OMIM: "Tremor (1 patient)" [OMIM:Tremor (1 patient)]
OMIM: "Tremor (3 patients)" [OMIM:Tremor (3 patients)]
OMIM: "Tremor (30%)" [OMIM:Tremor (30%)]
OMIM: "Tremor (57% of patients)" [OMIM:Tremor (57% of patients)]
OMIM: "Tremor (in some patients)" [OMIM:Tremor (in some patients)]
OMIM: "Tremor (later-onset)" [OMIM:Tremor (later-onset)]
OMIM: "Tremor (less common)" [OMIM:Tremor (less common)]
OMIM: "Tremor (rare)" [OMIM:Tremor (rare)]
OMIM: "Tremor, fine" [OMIM:Tremor, fine]
OMIM: "Tremors" [OMIM:Tremors]
OMIM: "Tremors (in hands)" [OMIM:Tremors (in hands)]
UMLS:C1963252 "Tremor" [HPO:0001337]
UMLS:C0040822 "Tremor" [Orphanet:43240]
Is a (Direct Parents):
MedDRA Abnormality of movement
HPO         Tremor by anatomical site
HPO         Abnormality of movement
Orphanet Abnormality of movement
HPO         Rubral tremor
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 movement(HPO:0100022)
                Tremor(HPO:0001337)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Tremor(HPO:0001337)
Database Frequency: 200 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
4q21 microdeletion syndrome (Orphanet:238750)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
AICARDI-GOUTIERES SYNDROME 6 (OMIM:615010)
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY (OMIM:614307)
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
ATAXIA-TELANGIECTASIA (OMIM:208900)
ATTRV122I amyloidosis (Orphanet:85451)
Aceruloplasminemia (Orphanet:48818)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Adult-onset dystonia-parkinsonism (Orphanet:199351)
Alexander disease (Orphanet:58)
Alpers syndrome (Orphanet:726)
Ataxia - oculomotor apraxia type 1 (Orphanet:1168)
Ataxia with vitamin E deficiency (Orphanet:96)
Ataxia-telangiectasia (Orphanet:100)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Atypical progressive supranuclear palsy (Orphanet:99750)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant focal dystonia, DYT7 type (Orphanet:93963)
Autosomal dominant optic atrophy and cataract (Orphanet:67036)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal recessive ataxia due to ubiquinone deficiency (Orphanet:139485)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive dopa-responsive dystonia (Orphanet:101150)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
Benign adult familial myoclonic epilepsy (Orphanet:86814)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3 (OMIM:613227)
CLN13 disease (Orphanet:352709)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18 (OMIM:615578)
CREST syndrome (Orphanet:90290)
Cabezas syndrome (Orphanet:85293)
Cataract - ataxia - deafness (Orphanet:1368)
Cerebellar hypoplasia - tapetoretinal degeneration (Orphanet:2246)
Cerebrotendinous xanthomatosis (Orphanet:909)
Choreoacanthocytosis (Orphanet:2388)
Chédiak-Higashi syndrome (Orphanet:167)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Classic galactosemia (Orphanet:79239)
Classical phenylketonuria (Orphanet:79254)
Classical progressive supranuclear palsy (Orphanet:240071)
Coats plus syndrome (Orphanet:313838)
Cockayne syndrome (Orphanet:191)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Complete androgen insensitivity syndrome (Orphanet:99429)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency (Orphanet:93583)
DPAGT1-CDG (Orphanet:86309)
DPM1-CDG (Orphanet:79322)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
Dehydratase deficiency (Orphanet:1578)
Dihydropteridine reductase deficiency (Orphanet:226)
Distal hereditary motor neuropathy type 7 (Orphanet:139589)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY (OMIM:615924)
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 (OMIM:607876)
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3 (OMIM:613608)
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 (OMIM:615400)
EPILEPSY, PROGRESSIVE MYOCLONIC 7 (OMIM:616187)
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B (OMIM:612437)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 (OMIM:612164)
Early-onset X-linked optic atrophy (Orphanet:98890)
Early-onset generalized limb-onset dystonia (Orphanet:256)
Episodic ataxia type 1 (Orphanet:37612)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial dementia, British type (Orphanet:97345)
Familial or sporadic hemiplegic migraine (Orphanet:569)
Familial sick sinus syndrome (Orphanet:166282)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
GM1 gangliosidosis (Orphanet:354)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Galactosemia (Orphanet:352)
Gaucher disease (Orphanet:355)
Gaucher disease type 3 (Orphanet:77261)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Hemochromatosis type 4 (Orphanet:139491)
Hereditary continuous muscle fiber activity (Orphanet:972)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperlysinemia, type I (OMIM:238700)
Hypomyelination with atrophy of basal ganglia and cerebellum (Orphanet:139441)
Infantile dystonia-parkinsonism (Orphanet:238455)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Joubert syndrome (Orphanet:475)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Joubert syndrome with renal defect (Orphanet:220497)
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency (Orphanet:352497)
Kallmann syndrome (Orphanet:478)
Kennedy disease (Orphanet:481)
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS (OMIM:614561)
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE (OMIM:615889)
Leber plus disease (Orphanet:99718)
Leigh syndrome (Orphanet:506)
Leukoencephalopathy - metaphyseal chondrodysplasia (Orphanet:83629)
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation (Orphanet:137898)
Lower motor neuron syndrome with late-adult onset (Orphanet:276435)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6 (OMIM:611092)
MERRF (Orphanet:551)
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 (OMIM:141500)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
MYOPATHY WITH EXTRAPYRAMIDAL SIGNS (OMIM:615673)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Monomelic amyotrophy (Orphanet:65684)
Monosomy 18q (Orphanet:1600)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Multiple system atrophy (Orphanet:102)
Myoclonus-dystonia syndrome (Orphanet:36899)
NEMALINE MYOPATHY 5 (OMIM:605355)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA (OMIM:158580)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Neuroferritinopathy (Orphanet:157846)
Niemann-Pick disease type C (Orphanet:646)
Nipah virus disease (Orphanet:99825)
Ornithine transcarbamylase deficiency (Orphanet:664)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PARALYSIS AGITANS, JUVENILE, OF HUNT (OMIM:168100)
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO (OMIM:610297)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:260300)
PARKINSON DISEASE 17 (OMIM:614203)
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE (OMIM:600116)
PARKINSON DISEASE 20, EARLY-ONSET (OMIM:615530)
PELIZAEUS-MERZBACHER DISEASE (OMIM:312080)
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS (OMIM:614369)
PEROXISOME BIOGENESIS DISORDER 5B (OMIM:614867)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Parkinsonian-pyramidal syndrome (Orphanet:171695)
Peripartum cardiomyopathy (Orphanet:563)
Perry syndrome (Orphanet:178509)
Primary dystonia, DYT13 type (Orphanet:98807)
Primary dystonia, DYT2 type (Orphanet:99657)
Primary orthostatic tremor (Orphanet:238606)
Progressive myoclonic epilepsy type 6 (Orphanet:280620)
Progressive supranuclear palsy - parkinsonism (Orphanet:240085)
Proximal myotonic myopathy (Orphanet:606)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Rett syndrome (Orphanet:778)
Riboflavin transporter deficiency (Orphanet:97229)
SPINOCEREBELLAR ATAXIA 37 (OMIM:615945)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 (OMIM:615768)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
Scrub typhus (Orphanet:83317)
Sensorineural hearing loss - early graying - essential tremor (Orphanet:66633)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Sneddon syndrome (Orphanet:820)
Spastic paraparesis - deafness (Orphanet:2815)
Spinocerebellar ataxia type 18 (Orphanet:98771)
Spinocerebellar ataxia type 23 (Orphanet:101108)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Spinocerebellar ataxia type 8 (Orphanet:98760)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Spontaneous periodic hypothermia (Orphanet:29822)
Sézary syndrome (Orphanet:3162)
TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS (OMIM:611808)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
Tremor - nystagmus - duodenal ulcer (Orphanet:3350)
Triose phosphate-isomerase deficiency (Orphanet:868)
Trisomy X (Orphanet:3375)
Typhoid (Orphanet:99745)
Tyrosinemia type 2 (Orphanet:28378)
Tyrosinemia type 3 (Orphanet:69723)
Urocanic aciduria (Orphanet:210128)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-responsive methylmalonic acidemia type cblA (Orphanet:79310)
Williams syndrome (Orphanet:904)
Wilson disease (Orphanet:905)
Wolfram syndrome 1 (OMIM:222300)
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)
X-linked dystonia-parkinsonism (Orphanet:53351)
X-linked spinocerebellar ataxia type 4 (Orphanet:85292)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Xeroderma pigmentosum complementation group G (Orphanet:276267)