Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 47% —
Register , to see more distinctive signs of diseases and studies — 35%
dilated cardiomyopathy
45%
—
hepatosplenomegaly —
27%
ventricular paroxysmal tachycardia
45%
—
enlargement of the liver and spleen —
27%
ventricular fibrillation
42%
—
enlargement of the spleen —
26%
sudden cardiac death
41%
—
difficult to swallow —
26%
tachycardia attacks
39%
—
niemann-pick disease —
26%
arrhythmia tachycardia
38%
—
childhood diseases
12%
36%
violation of the right departments hearts
37%
—
enlarged liver —
24%
history of myocardial infarction
37%
—
gaucher's disease —
24%
cardiac arrest
37%
—
rashes dry —
23%
ventricular flutter
36%
—
porous skin —
23%
violation of the left parts of the heart
36%
—
wolman 's disease —
23%
brugada syndrome
35%
—
volume of spleen is increased —
22%
the syndrome of the shortened qt interval
35%
—
narcolepsy —
22%
sudden tachycardia
34%
—
lags behind in the development —
22%
fainting
33%
—
angioceratoma —
22%
acute coronary syndrome
33%
—
fabry's disease —
22%
sudden heartbeat
32%
—
the onset of the disease during puberty —
21%
ventricular extrasystole
31%
—
increased LDL —
21%
disorders of consciousness
31%
—
liver problems —
21%
bradycardia
31%
—
portal hypertension —
21%
hypertrophic cardiomyopathy
41%
8%
hypersplenism —
21%
restrictive cardiomyopathy
40%
8%
alt reduction —
20%
cardiomyopathy
39%
7%
muscle weakness —
20%
extrasystole
28%
—
onset of illness
5%
25%
parasystole
28%
—
reduction of HDL —
20%
long qt syndrome
27%
—
increased HDL —
20%
heart defect
27%
—
reduction of ast —
19%
arrhythmia attacks
38%
10%
increased cholesterol levels in the blood —
19%
angina attack
25%
—
familial endogenous hypertriglyceridemia —
19%
cardiac asthma
25%
—
reduction of LDL —
19%
wolf-parkinson-white syndrome
25%
—
macrocephaly —
19%
left-sided symptoms
25%
—
congenital liver fibrosis —
19%
tachycardia
33%
6%
cholestasis —
19%
heart disease in the genus
24%
—
slowness of movement —
19%
left ventricular aneurysm
24%
—
liver transplantation —
19%
palpitations
32%
6%
enteropathy —
18%
angina pectoris
33%
7%
malabsorption —
18%
permanent arrhythmia
33%
7%
thrombocytopenia —
18%
clinical death
23%
—
progressive supranuclear paralysis —
18%
andersen syndrome
23%
—
splenectomy —
18%
nose pulmonary heart
30%
6%
history of liver surgery —
18%
heart hypertrophy
39%
15%
impaired spleen function —
18%
duration of st segment is increased
22%
—
lower cholesterol —
18%
decreased potassium
22%
—
primary hypercholesterolemia —
18%
omission of internal organs
22%
—
liver failure —
18%
sarcoidosis
22%
—
dry —
18%
myocardial revascularization
22%
—
rupture duodenal dysfunction —
17%
congestion belching
22%
—
expansion of the esophagus —
17%
ecg without pathology
22%
—
hemorrhagic diathesis —
17%
cardiodilation
33%
9%
cardiac cirrhosis of the liver —
17%
periodic fainting
21%
—
sluggish baby —
17%
fainting in childhood
21%
—
liver dysfunction —
17%
ischemic cardiomyopathy
21%
—
congenital anomalies of the lower extremities —
17%
tachycardia in the morning
21%
—
intestinal insufficiency syndrome —
17%
increase in magnesium
21%
—
hepatosis fatty —
17%
parkinson's disease
21%
—
leukopenia —
17%
infections palpitations in the morning
20%
—
hepatosis —
17%
blockade of the legs of the bundle of gis
20%
—
adynamia —
17%
myocarditis
20%
—
epilepsy in the morning —
17%
mitral valve
20%
—
epilepsy attacks
10%
27%
atrioventricular block
30%
8%
chronic venous edema —
16%
tachycardia under stress
20%
—
affective disorders —
16%
palpitations under stress
19%
—
cirrhosis of the liver —
16%
decreased magnesium
19%
—
ascites —
16%
reperfusion syndrome
19%
—
anemia —
16%
heaviness on the heart
19%
—
calcification —
16%
heart disease in relatives
19%
—
need for fats —
16%
magnesia
18%
—
kidney transplantation —
16%
myocardial infarction
33%
13%
abdominal pain —
16%
constant heartbeat
18%
—
effects of puberty —
16%
pacemaker
18%
—
liver atrophy —
16%
acute left ventricular failure
18%
—
corneal opacity —
16%
acute condition
26%
6%
swelling of the legs —
16%
heart transplantation
18%
—
dyslipidemia —
16%
constant tachycardia
18%
—
polyneuropathy —
16%
scarring
17%
—
general swelling does —
16%
head established magnesium deficiency
17%
—
hypertrophy biliary tract —
16%
hypomagnesemia
17%
—
muscular dystonia —
16%
shortened cycle
17%
—
infantile —
16%
arrhythmia
34%
16%
blindness —
16%
pericarditis
16%
—
quickly gets tired —
16%
frequent dizziness
16%
—
neurogenic pain —
15%
dizziness when getting
16%
—
hemophagocytic syndrome —
15%
steinert 's disease
16%
—
2 children —
15%
hyperventilation syndrome
16%
—
memory impairment —
15%
muscular dystrophy
16%
—
pathological fracture —
15%
convulsions with loss of consciousness
16%
—
abdominal swelling —
15%
caution
16%
—
anomalies of esophageal development —
15%
secondary cardiomyopathy
16%
—
neurological pain —
15%
aldosteroma
16%
—
abdominal pain after diarrhea —
15%
organophosphate poisoning
16%
—
nose nursing mom —
15%
after heart surgery
15%
—
increased bleeding —
15%
pre-fainting condition
24%
7%
steatorrhea —
15%
pain in the sternum
15%
—
metabolic disorder
13%
28%
refuses treatment
15%
—
history of surgery
16%
31%
consequences of physical exertion
15%
—
limbs pain —
15%
anorexia nervosa
15%
—
fever intermittent —
14%
progressive duchenne muscular dystrophy
15%
—
a difficult teenager —
14%
pain when touched
15%
—
stomach bloating strong —
14%
feeling of electricity
15%
—
chills in the afternoon —
14%