Vertigo
Symptom Information:
Symptom ID: | HPO:0002321 | |||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 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) Coordination and balance disturbances(MedDRA:10072984) Vertigo(HPO:0002321) Neurological signs and symptoms NEC(MedDRA:10029306) Vertigo(HPO:0002321) Vertigos NEC(MedDRA:10052769) Vertigo(HPO:0002321) |
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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) |