Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 50% —
Register , to see more distinctive signs of diseases and studies — 34%
ipex syndrome
32%
—
cardiomyopathy —
27%
polyuria
28%
—
pompe disease —
26%
urination with blood
22%
—
muscle weakness —
24%
autoimmune insulin syndrome
20%
—
there is heart failure —
22%
dehydration
20%
—
heart failure —
22%
high thin
19%
—
sluggish baby —
22%
abnormalities of pancreatic development
18%
—
heart dysfunction —
22%
history medical mother's
16%
—
cardiomyopathy in children —
21%
spondyloepiphyseal dysplasia
16%
—
enlargement of the heart —
21%
pancreatopathy
16%
—
cardiodilation —
20%
ketonuria
15%
—
nose nursing mom —
19%
dehydration in children
15%
—
weak heart —
19%
appetite is preserved
15%
—
liver problems —
19%
mom has diabetes
14%
—
history of surgery —
19%
enterovirus infection
14%
—
infantile —
19%
increased diuresis
14%
—
weakness in the heart —
19%
thyroiditis
14%
—
angioplasty —
19%
very dry skin
14%
—
gierke's disease —
18%
autoimmune thyroiditis
14%
—
impaired lung function —
18%
chronic eczema
14%
—
respiratory insufficiency —
18%
diabetes mellitus
21%
6%
onset of illness —
18%
hemolytic anemia
13%
—
lactic acidosis —
17%
mitochondrial myopathy
13%
—
hypoglycemic coma —
17%
child's poor appetite
13%
—
increase in creatine kinase —
17%
thin child
13%
—
inflammation —
16%
viral diarrhea
13%
—
dystrophy —
16%
hypersthenuria
13%
—
nephronophthys fanconi —
16%
diabetes mellitus in children
13%
—
enlargement of the spleen —
16%
hyperglycemia
24%
9%
myopathy
11%
26%
fussy child
12%
—
osteoporosis —
15%
eats everything
12%
—
weakness in the hands —
15%
periodic weakness
12%
—
weakness of the muscles of the hands —
15%
appetite is poor
12%
—
kidney transplantation —
14%
adynamia
12%
—
renal tubular acidosis —
14%
eczema
12%
—
exhaustion —
14%
insulin deficiency
12%
—
osteopenia —
14%
familial diabetes
12%
—
benign epithelial tumors —
14%
dependence on parents
11%
—
diseases of infants —
14%
sensitive child
11%
—
muscular dystrophy —
14%
no feeling of hunger
11%
—
kidney stones —
14%
immaturity
11%
—
muscle atrophy —
14%
dry skin
11%
—
family man —
13%
heredity predisposition
10%
—
complication of acute respiratory viral infections —
13%
enteropathy
10%
—
reduction of the number of movements (oligokinesia) —
13%
no appetite
10%
—
renal osteodystrophy —
13%
general weakness
10%
—
weakness in the legs —
13%
periods of exacerbation
17%
5%
increased uric acid —
13%
smell of acetone from the mouth
17%
8%
masked face (hypomimia) —
13%
thin
17%
9%
exhaustion after illness —
13%
bad breath unpleasant
13%
6%
arterial hypertension in children —
13%
type 1 diabetes mellitus
11%
5%
weakness in the leg muscles —
13%
delay in physical development
11%
5%
liver atrophy —
13%
chronic diarrhea
12%
6%
arterial hypertension of the III degree —
13%
little low energy level
12%
6%
chronic liver failure —
13%
unformed feces
14%
8%
facial muscle weakness —
13%
dry
9%
4%
liver transplantation —
13%
hormonal disorders
9%
4%
enlarged liver
10%
23%
diarrhea
13%
8%
weakness after illness
9%
22%
periodic illness
15%
11%
headache with a cold —
13%
hematuria
9%
5%
hypotrophy —
12%
lags behind in the development
16%
12%
headache pain in the morning —
12%
neutropenia —
12%
chronic heart failure —
12%
liver failure —
12%
weakness in the arms and legs —
12%
effects of puberty —
12%
qrs interval duration lowered —
12%
density is increased —
12%
increased pressure in the morning —
12%
hepatosis fatty —
12%
hyperlipidemia —
12%
swelling of the tongue —
12%
stunting —
12%
cholesterolemia —
12%
protein c deficiency —
12%
neurological disorders —
12%
history of liver surgery —
12%
growth disorders in children —
12%
hyperechoic liver —
11%
red tip of the nose —
11%
pq interval duration is lowered —
11%
CHD —
11%
nephropathy —
11%
there is hypertension in the family —
11%
fasting —
11%
weakness in the extremities —
11%
inflammatory bowel diseases —
11%
weak lungs —
11%
hepatosis —
11%
heart hypertrophy —
11%
consequences of taking medications —
11%
liver cancer —
11%
weakness in the shoulder —
11%
cirrhosis of the liver —
11%
liver dysfunction —
11%
drug disease —
11%
intestinal mucosa —
11%
pancreas hyperechoic —
11%
tearfulness —
11%
lung pain —
10%
benign neoplasms —
10%
eats slowly —
10%
delay of mental development —
10%
duck gait —
10%
macroglossia —
10%
amyloidosis of the kidneys —
10%
hypotension with weakness —
10%
pale skin —
10%
delayed speech development —
10%
frequent otitis —
10%
increased ast —
10%
anechoic liver —
10%
gout of the joints —
10%
difficult to swallow —
10%
chronic gouty arthritis —
10%
protein reduced —
10%
hypotension —
10%
ARVI —
10%
duration of pq interval is increased —
10%
is gaining weight poorly —
10%
loss of balance —
10%
children's speech —
10%
essential hypertension —
10%
convulsions —
10%
familial hypertension —
10%
metabolic myopathy —
10%
nephrosis —
10%
intestinal insufficiency syndrome —
10%
increased alt —
10%
duration of qrs interval is increased —
10%
pain when breathing —
10%
impaired arterial function —
10%
diseases of the gastrointestinal tract —
10%
dysfunction of the gallbladder —
10%
lot of operations in small things —
9%
dilated cardiomyopathy —
9%
gout —
9%
weak ligaments —
9%
headaches —
9%