Vertigo

Symptom Information:

Symptom ID: HPO:0002321
Synonyms:
Dizziness [HPO:0002321]
Dizziness [Orphanet:13620]
Dizziness and giddiness (finding) [Orphanet:13620]
Subjective vertigo (finding) [Orphanet:13620]
Giddiness (finding) [Orphanet:13620]
Dizziness (finding) [Orphanet:13620]
Dizziness and giddiness symptoms [Orphanet:13620]
Dysequilibrium [Orphanet:13620]
giddiness, vertigo [Orphanet:13620]
Dizziness [OMIM:Dizziness]
Vertigo [OMIM:Vertigo]
Giddiness [Orphanet:13620]
Dizziness [MedDRA:10013573]
Dizziness (excl vertigo) [MedDRA:10013573]
Dizziness and giddiness [MedDRA:10013573]
Dizzy [MedDRA:10013573]
Dizzy spells [MedDRA:10013573]
Faintness [MedDRA:10013573]
Felt faint [MedDRA:10013573]
Felt giddy [MedDRA:10013573]
Giddiness [MedDRA:10013573]
Light headedness [MedDRA:10013573]
Light-headed [MedDRA:10013573]
Light-headed feeling [MedDRA:10013573]
Lightheadedness [MedDRA:10013573]
Swaying feeling [MedDRA:10013573]
Wooziness [MedDRA:10013573]
Woozy [MedDRA:10013573]
Dizziness aggravated [MedDRA:10013573]
Balance disorder [MedDRA:10049848]
Balance difficulty [MedDRA:10049848]
Balance impaired NOS [MedDRA:10049848]
Disequilibrium syndrome [MedDRA:10049848]
Disorder equilibrium [MedDRA:10049848]
Dysequilibrium [MedDRA:10049848]
Equilibrium disorder of (NOS) [MedDRA:10049848]
Unsteadiness [MedDRA:10049848]
Equilibrium loss [MedDRA:10049848]
Equilibrium trouble [MedDRA:10049848]
Impairment of balance (finding) [Orphanet:43210]
Problem with balance (finding) [Orphanet:43210]
Equilibration disorder [Orphanet:43210]
Dysequilibrium [Orphanet:43210]
Ataxia/incoordination/trouble of the equilibrium [Orphanet:43210]
Vertigo [MedDRA:10047340]
Quality:
Cross references:
HPO:0002141 "Gait imbalance" [Orphanet:13620]
Orphanet:13620 "Dizziness" [Orphanet:13620]
Orphanet:43210 "Ataxia/incoordination/trouble of the equilibrium" [Orphanet:43210]
OMIM: "Dizziness" [OMIM:Dizziness]
OMIM: "Vertigo" [OMIM:Vertigo]
UMLS:C0042571 "Vertigo" [HPO:0002321]
UMLS:C0476206 "Dizziness and giddiness symptoms" [Orphanet:13620]
UMLS:C0281825 "Dysequilibrium" [Orphanet:13620]
UMLS:C0012833 "Dizziness" [Orphanet:13620]
UMLS:C0476207 "giddiness, vertigo" [Orphanet:13620]
UMLS:C0575090 "Equilibration disorder" [Orphanet:43210]
UMLS:C0281825 "Dysequilibrium" [Orphanet:43210]
Is a (Direct Parents):
Orphanet [DEL]Motor deficit/trouble
Orphanet Functional anomalies of the inner ear
MedDRA Neurological signs and symptoms NEC
MedDRA Coordination and balance disturbances
HPO         Vestibular dysfunction
MedDRA Vertigos NEC
Orphanet Ataxia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the inner ear(HPO:0000359)
             Functional abnormality of the inner ear(HPO:0011389)
                Vestibular dysfunction(HPO:0001751)
                   Vertigo(HPO:0002321)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Neurological signs and symptoms NEC(MedDRA:10029306)
          Vertigo(HPO:0002321)
       Vertigos NEC(MedDRA:10052769)
          Vertigo(HPO:0002321)
       Coordination and balance disturbances(MedDRA:10072984)
          Vertigo(HPO:0002321)
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 3 (Orphanet:67047)
48,XXYY syndrome (Orphanet:10)
AL amyloidosis (Orphanet:85443)
Aceruloplasminemia (Orphanet:48818)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Argininosuccinic aciduria (Orphanet:23)
Arnold-Chiari malformation type I (Orphanet:268882)
Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
Benign familial mesial temporal lobe epilepsy (Orphanet:163717)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (Orphanet:293955)
DEAFNESS, AUTOSOMAL DOMINANT 11 (OMIM:601317)
DEAFNESS, AUTOSOMAL DOMINANT 9 (OMIM:601369)
DEAFNESS, AUTOSOMAL RECESSIVE 2 (OMIM:600060)
Desquamative interstitial pneumonia (Orphanet:98852)
Episodic ataxia type 1 (Orphanet:37612)
Episodic ataxia type 3 (Orphanet:79135)
Episodic ataxia type 4 (Orphanet:79136)
Episodic ataxia type 7 (Orphanet:209970)
Fabry disease (Orphanet:324)
Familial paroxysmal ataxia (Orphanet:97)
Familial progressive cardiac conduction defect (Orphanet:871)
HERNS syndrome (Orphanet:63261)
HYPOMAGNESEMIA 6, RENAL (OMIM:613882)
Hereditary continuous muscle fiber activity (Orphanet:972)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Kearns-Sayre syndrome (Orphanet:480)
Leber plus disease (Orphanet:99718)
Leigh syndrome (Orphanet:506)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 (OMIM:602481)
Maple syrup urine disease (Orphanet:511)
Maternally-inherited diabetes and deafness (Orphanet:225)
Meniere disease (Orphanet:45360)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Niemann-Pick disease type C (Orphanet:646)
Peripartum cardiomyopathy (Orphanet:563)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary familial polycythemia (Orphanet:90042)
Primary systemic amyloidosis (Orphanet:314701)
SYNCOPE, FAMILIAL VASOVAGAL (OMIM:609289)
Senile systemic amyloidosis (Orphanet:330001)
Sino-auricular heart block (Orphanet:1260)
Sinus node disease and myopia (OMIM:182190)
Sneddon syndrome (Orphanet:820)
Torsade-de-pointes syndrome with short coupling interval (Orphanet:51084)
Tyrosinemia type 2 (Orphanet:28378)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 (OMIM:614916)
VERTIGO, BENIGN RECURRENT (OMIM:193007)
Von Hippel-Lindau disease (Orphanet:892)
Wilson disease (Orphanet:905)
Wilson-Turner syndrome (Orphanet:3459)
Wolfram syndrome (Orphanet:3463)