Distinctive symptoms
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paralysis of the upper eyelids
67%
—
epilepsy —
42%
myoclonic dystonia
67%
—
liver diseases —
37%
parkinson's disease
66%
—
epileptiform seizures —
37%
dystonia
62%
—
tonic-clonic seizures —
34%
tremor
58%
—
clonic cramps —
33%
juvenile parkinsonism
56%
—
generalized epilepsy —
33%
alzheimer's disease
55%
—
shaky gait —
32%
periodic paralysis
54%
—
delayed digestion —
32%
paralysis
54%
—
hypoechoic liver —
30%
postural tremor
53%
—
prothrombin index lowered —
30%
dementia
48%
—
epileptic encephalopathy in children —
30%
gallervorden-spatz disease
46%
—
fine motor skills are impaired —
29%
twitching of the upper eyelid
68%
23%
crumpy syndrome —
29%
twitches eyelid
68%
23%
toxic liver —
29%
hyperkinesis
43%
—
nosebleed —
29%
dementia with lewy bodies
42%
—
hyperechoic liver —
29%
frontotemporal dementia
42%
—
worse when walking —
28%
stiffness in the joints
42%
—
liver failure —
28%
tics
64%
21%
neurological disorders —
28%
athetosis
40%
—
high temperature —
28%
shuffling gait
39%
—
encephalopathy —
28%
vascular parkinsonism
39%
—
polyneuropathy —
28%
lot paralysis left-sided
38%
—
epilepsy attacks —
28%
muscle tension
37%
—
cirrhosis of the liver —
28%
violations of the motor act
36%
—
childhood diseases —
27%
twitching limbs
36%
—
juvenile absentee epilepsy —
27%
secondary parkinsonism
36%
—
toxic hepatitis —
27%
weakness in the evening
36%
—
bleeding from the gums —
27%
paresis
35%
—
nosebleed —
27%
speech slurred
35%
—
cortical blindness —
26%
asymmetry
35%
—
biliary cirrhosis of the liver —
26%
upper paraparesis
35%
—
cramp and spasm —
25%
masked face (hypomimia)
34%
—
hepatitis —
25%
abasia
34%
—
migraine —
24%
eye tic
34%
—
pulmonary hemorrhage —
24%
involuntary movements
33%
—
mitochondrial myopathy —
24%
cramps in the extremities
33%
—
hepatic encephalopathy —
24%
ophthalmoplegia
33%
—
epilepsy in children —
23%
tremor of the limb
33%
—
febrile body temperature —
22%
peak's disease
33%
—
hyperbilirubinemia —
22%
numbness of the hands
33%
—
intellectual disabilities in children —
22%
chorea
33%
—
hypoproteinemia —
21%
limitation of the amplitude of movements
32%
—
myopathies —
21%
clumsiness
32%
—
smart baby —
21%
paralysis of the limbs
32%
—
tingling —
20%
slowness of movement (bradykinesia)
31%
—
blindness —
20%
decreased skin sensitivity
31%
—
hypoglycemia —
20%
violation of protein metabolism
31%
—
febrile —
20%
cerebellar ataxia
30%
—
liver dysfunction —
20%
contractures of the joints
30%
—
leg cramps —
20%
aphasia
30%
—
enlarged liver —
19%
discirculatory encephalopathy
30%
—
deterioration during pregnancy —
19%
contractures
28%
—
constant weakness —
19%
paralytic syndrome
28%
—
worse pregnancy —
19%
brain tumor
27%
—
pulsates —
19%
vascular sclerosis
27%
—
hypertrophy biliary tract —
19%
restriction of movement
27%
—
lung pain —
19%
protein-energy deficiency
27%
—
full —
19%
ataxia
26%
—
visual impairment —
18%
protein reduced
26%
—
digestive disorders —
18%
motor activity
26%
—
general loss of strength —
18%
cognitive disorders
25%
—
no appetite —
18%
atherosclerosis of blood vessels
25%
—
family man —
18%
protein c deficiency
25%
—
quickly gets tired —
17%
cerebral circulation disorder
25%
—
spasm —
17%
brain tumor
25%
—
feeling of bruising —
17%
need for activity
25%
—
metabolic disorder —
17%
organic brain damage
24%
—
subacute condition —
17%
muscle weakness
23%
—
nausea —
17%
damage to the nervous system
47%
22%
bleeding —
16%
weakness after illness
22%
—
pregnancy —
16%
up circulatory disorders
22%
—
onset of illness —
15%
strong man
22%
—
weakness
21%
—
angiopathy
21%
—
oncology
20%
—
skin problems
20%
—
ganglia
41%
22%
impaired coordination
43%
26%
skin anesthesia
34%
18%
insensitivity to pain
32%
17%
patient's condition
28%
15%
convulsions
51%
38%
loss of balance
38%
28%
hypoxia
23%
17%