Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 75% 19%
Register , to see more distinctive signs of diseases and studies — 55%
weakness
61%
23%
veins bloating —
53%
increase in creatine kinase
27%
—
increased ESR —
51%
fasting
22%
—
touchy —
45%
mitochondrial myopathy
22%
—
there is no thirst —
44%
sweating legs
21%
—
chronic condition
11%
54%
duck gait
20%
—
niemann-pick disease —
43%
dilated cardiomyopathy
20%
—
impaired lung function
20%
62%
ray 's syndrome
20%
—
of the desire for fresh air —
42%
can't walk
19%
—
burning in the feet —
41%
smell of sweat unpleasant
19%
—
gaucher's disease —
41%
becker's progressive muscular dystrophy
18%
—
lipoidosis —
40%
leg weakness walking
18%
—
patient's condition
12%
51%
rhabdomyolysis
17%
—
mch increased —
37%
nemaline myopathy
17%
—
angioceratoma —
37%
metabolic myopathy
17%
—
another refined dermatitis —
37%
alcoholic myopathy
17%
—
fabry's disease —
36%
hyperammonemia
17%
—
hepatosplenomegaly —
36%
myopathies
30%
12%
impaired spleen function —
35%
hellp syndrome
16%
—
enlargement of the spleen
5%
39%
lethargy
16%
—
worse in morning —
34%
congenital myopathies
16%
—
mchc reduced —
32%
myoglobinuria
16%
—
enlargement of the liver and spleen
5%
37%
oppenheim syndrome
16%
—
tinnitus —
31%
no strength
16%
—
nervous excitability
7%
36%
ganglioneuritis
15%
—
varicose veins of the legs —
29%
sudden infant death syndrome
15%
—
increase ggtp —
29%
thyroid is enlarged to 3 deg
15%
—
hypertension
4%
32%
viral diarrhea
15%
—
veins swelling on the legs —
28%
muscle fatigue
15%
—
hot —
27%
muscle atrophy
15%
—
leukopenia —
27%
acute liver failure
15%
—
reddening of the skin —
26%
dystrophy
20%
4%
increased cholesterol —
25%
motor activity
14%
—
enlarged liver
11%
36%
sucks in the stomach
14%
—
pneumosclerosis —
24%
death of the child
13%
—
wolman 's disease —
24%
contractures of the joints
13%
—
interstitial lung diseases —
23%
metabolic acidosis
13%
—
febrile —
23%
progressive bulbar paralysis
13%
—
interstitial pneumonia —
23%
scoliosis
13%
—
rash like urticaria —
23%
deformations of the feet
13%
—
fermentopathy —
22%
muscular dystrophy
13%
—
hyperactive child
9%
31%
enterovirus infection in children
13%
—
hypersplenism —
21%
lethargy drowsiness
13%
—
impressionability —
21%
spinal fracture
13%
—
rashes dry —
20%
of medica matter
13%
—
hyperactive
8%
28%
violation of protein metabolism
12%
—
portal hypertension —
20%
striae
12%
—
limbs pain —
20%
weakness during the day
12%
—
volume of spleen is increased —
20%
ones weakness after eating
12%
—
arthropathy —
19%
parametrite
12%
—
atherosclerosis of blood vessels —
19%
coma
12%
—
sarcoidosis of the skin —
19%
increased potassium
12%
—
fast saturation —
19%
hyperinsulinism
12%
—
heerfordt syndrome —
19%
infectious myelopathy
12%
—
neurogenic pain —
19%
spondylopathy
12%
—
pain in the spleen —
19%
scleroderma in children
12%
—
increased LDL —
18%
trichinosis
12%
—
cataplexy —
18%
history medical mother's
12%
—
worse from cold —
18%
curvature of the spine
12%
—
reduction of HDL —
18%
alimentary dystrophy
12%
—
increased HDL —
18%
paralysis
12%
—
the onset of the disease during puberty —
18%
weakness in the legs
22%
8%
pain in the wrists —
18%
the child does not eat
11%
—
pregnancy
14%
32%
dystrophy in children
11%
—
dyslipidemia
8%
26%
the feeling of parasites
11%
—
type 2 diabetes mellitus
6%
24%
vascular myelopathy
11%
—
hyperbilirubinemia —
17%
vomiting with blood
11%
—
sarcoidosis of the lungs —
17%
chronic bronchitis unspecified
11%
—
sweating
5%
22%
atrophoderma
11%
—
reduction of ast —
17%
polymyositis
11%
—
childhood diseases
19%
36%
better when walking
11%
—
pain in the legs —
17%
keratitis in children
11%
—
alt reduction —
17%
viral endocarditis
11%
—
tetraparesis —
17%
chronic obstructive bronchitis
11%
—
reduced sweating —
17%
glutaric aciduria
11%
—
pain in the arms and legs —
17%
flu
11%
—
deafness —
17%
restriction of movement
11%
—
pain pain in the bones —
17%
coma in a child
11%
—
with anemia
5%
22%
hypoglycemic coma
11%
—
cardiac cirrhosis of the liver —
17%
ketonuria
11%
—
leukodystrophy —
17%
increased uric acid
11%
—
nodular erythema —
17%
macular
11%
—
ataxia
5%
22%
rapid breathing
11%
—
reduction of LDL —
17%
Chronical bronchitis
11%
—
hemorrhagic diathesis —
17%
feeling of a coma in the stomach
11%
—
bruises do not go away for a long —
16%
a mobile child
11%
—
increased cholesterol levels in the blood —
16%
diencephalic syndrome
11%
—
familial endogenous hypertriglyceridemia —
16%
eats often
11%
—
sarcoidosis of the eyes —
16%
weak breathing
11%
—
paresis of the hand —
16%
bacterial keratitis
11%
—
bone necrosis —
16%
intensive physical load
11%
—
primary pulmonary hypertension —
16%
diarrhea with undigested food
11%
—
converging strabismus —
16%
vomiting bile in the morning
11%
—
of pure hypercholesterolemia —
16%
ones weakness in the leg muscles
22%
9%
congenital liver fibrosis —
16%
chronic liver failure
11%
—
cirrhosis of the liver —
16%
hiv infection in children
10%
—
pathological fracture —
16%
respiratory distress syndrome
10%
—
serum angiotensin-converting enzyme activity is increased —
16%
sweating with the smell
10%
—
poor sleep
7%
23%
masked face (hypomimia)
10%
—
aseptic bone necrosis —
16%
I'm being controlled
10%
—
pain in the foot —
16%