UMLS:C0042571 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0042571 (vertigo)
7,148 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
FAM136A	0.000
ENT	0.000
CACNA1A	0.000
MRI	0.000
MAS	0.000
EA2	0.000
Ankyrin repeat domain 30A	0.000
phosphate cytidylyltransferase 2, ethanolamine	0.000
otoconin 90	0.000
SEMA3D	0.000
Otolin-1	0.000
DTNA	0.000
OTOG	0.000
ENG	0.000
She	0.000
Stereocilin	0.000
FKBP3	0.000
ABR	0.000
TMEM55B	0.000
DFNA9	0.000
HMX2	0.000
CISS	0.000
STRC	0.000
MARVELD2	0.000
LIM homeobox transcription factor 1 alpha	0.000
SPBP	0.000
TSHZ1	0.000
VIII	0.000
COCH	0.000
PTA	0.000
WW domain containing E3 ubiquitin protein ligase 1	0.000
EAT-2	0.000
DFNA1	0.000
PXF	0.000
ESRRB	0.000
stereocilin	0.000
CACNB4	0.000
SCA6	0.000
SCN3B	0.000
CSF	0.000

Disease
Meniere's disease	0.028
Benign paroxysmal positional vertigo	0.028
nystagmus	0.019
vestibular neuritis	0.013
endolymphatic hydrops	0.007
neuronitis	0.006
sensorineural hearing loss	0.004
labyrinthitis	0.003
vertebrobasilar insufficiency	0.002
deafness	0.001
migraine	0.001
ear disease	0.001
Migrainous vertigo	0.001
Tullio phenomenon	0.001
Vestibular vertigo	0.001
facial palsy	0.001
Benign recurrent vertigo	0.001
Benign paroxysmal vertigo of childhood	0.001
acoustic neuroma	0.001
Benign paroxysmal vertigo	0.001
Vestibular disorders	0.001
motion sickness	0.001
diplopia	0.001
middle ear	0.001
Cogan's syndrome	0.001
Nystagmus	0.001
Acute vestibular syndrome	0.001
Perilymph fistula	0.001
basilar insufficiency	0.001
Wallenberg's syndrome	0.001
otosclerosis	0.000
Motor Disorders	0.000
interstitial keratitis	0.000
schwannoma	0.000
Central positional nystagmus	0.000
Vertical nystagmus	0.000
Basilar migraine	0.000
Recurrent vestibulopathy	0.000
vertebral artery syndrome	0.000
CAPA	0.000

Symptom
vertigo	1.000
tinnitus	0.026
dizziness	0.018
headache	0.002
nausea	0.002
ataxia	0.002
Cupulolithiasis	0.001
Acute vertigo	0.001
otalgia	0.001
vomiting	0.001
Spontaneous nystagmus	0.001
Vertigo/dizziness	0.001
dysarthria	0.001
lightheadedness	0.001
Sudden deafness	0.001
paresis	0.000
Ear symptoms	0.000
hyperacusis	0.000
ENT	0.000
blurred vision	0.000
bilateral carotid bruits	0.000
syncope	0.000
weakness	0.000
Matutinal vertigo	0.000
disturbed hearing	0.000
neck pain	0.000
numbness	0.000
bleeding from the lips	0.000
Secondary endolymphatic hydrops	0.000
diminished hearing	0.000
Drop attacks	0.000
giddiness	0.000
giddiness	0.000
paresthesia	0.000
ataxic gait	0.000
cerebellar ataxia	0.000
nausea and vomiting	0.000
Limb ataxia	0.000
Convulsive movements	0.000
Dizziness or vertigo	0.000

Enzyme
ascorbate oxidase	0.000
VOR	0.000
PTA	0.000
alpha-N-acetylgalactosaminidase	0.000
alpha-galactosidase	0.000
histidine decarboxylase	0.000
PHT	0.000
cellulose synthase	0.000
proteinase-3	0.000
biotinidase	0.000
choline kinase	0.000
CGT	0.000
cellulose synthase	0.000
ACE	0.000
gamma-glutamyl transpeptidase	0.000
MDH	0.000
methionine synthase	0.000
BAT	0.000
PAT	0.000
MDH	0.000
FFT	0.000
methionine synthase	0.000
3beta-hydroxysteroid dehydrogenase	0.000
glucose dehydrogenase	0.000
neuropathy target esterase	0.000
PCE	0.000
thyroid peroxidase	0.000
dopamine beta-hydroxylase	0.000
cholinesterase	0.000
indoleamine 2,3-dioxygenase	0.000
TOR	0.000
pyruvate dehydrogenase	0.000
pyruvate dehydrogenase	0.000
aldehyde dehydrogenase	0.000
MAT	0.000
tryptophan hydroxylase	0.000
tissue plasminogen activator	0.000
prostaglandin synthetase	0.000
aldehyde dehydrogenase	0.000
aldehyde dehydrogenase	0.000