Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 37% —
Register , to see more distinctive signs of diseases and studies — 50%
enuresis after midnight
35%
—
ipex syndrome —
32%
tubulopathy
32%
—
autoimmune insulin syndrome —
20%
liddle syndrome
31%
—
hyperglycemia
5%
24%
loves praise
29%
—
high thin —
19%
bartter syndrome
29%
—
abnormalities of pancreatic development —
18%
sentimental
28%
—
smell of acetone from the mouth —
17%
cystinosis
28%
—
periods of exacerbation —
17%
hypophosphatemia
27%
—
spondyloepiphyseal dysplasia —
16%
nephronophthys fanconi
27%
—
history medical mother's —
16%
aversion to criticism
27%
—
pancreatopathy —
16%
renal tubular acidosis
25%
—
ketonuria —
15%
rickets
24%
—
periodic illness —
15%
can't hold urine
23%
—
appetite is preserved —
15%
stubborn stubborn
23%
—
chronic eczema —
14%
urinary incontinence
22%
—
thyroiditis —
14%
nephropathy
22%
—
autoimmune thyroiditis —
14%
increased potassium
21%
—
very dry skin —
14%
increased sodium
21%
—
enterovirus infection —
14%
nephrogenic diabetes insipidus
21%
—
hemolytic anemia —
13%
indecision
21%
—
bad breath unpleasant —
13%
bradycardia
20%
—
viral diarrhea —
13%
nervousness
19%
—
thin child —
13%
phosphate-diabetes
17%
—
insulin deficiency —
12%
increase in phosphorus
17%
—
fussy child —
12%
metabolic alkalosis
16%
—
eczema —
12%
hyperaldosteronism
16%
—
little low energy level —
12%
phosphaturia
16%
—
chronic diarrhea —
12%
renal osteodystrophy
16%
—
adynamia —
12%
legs thick
16%
—
eats everything —
12%
rickets -like diseases
16%
—
periodic weakness —
12%
muscle weakness
16%
—
sensitive child —
11%
diabetes insipidus
16%
—
dry skin —
11%
galactosemia
16%
—
coma —
11%
alkalosis
15%
—
general weakness —
10%
tyrosinemia
15%
—
enlarged liver —
10%
saliva with blood
15%
—
heredity predisposition —
10%
gierke's disease
15%
—
dependence on the doctor —
9%
hypotension
15%
—
thin
8%
17%
renin lowered
14%
—
urination with blood
13%
22%
hypotonic dehydration
14%
—
unformed feces
5%
14%
poisoning with heavy metal salts
14%
—
mitochondrial myopathy
6%
13%
myeloma
13%
—
increased diuresis
7%
14%
no children
13%
—
mom has diabetes
7%
14%
auscultation of the heart
13%
—
polyuria
22%
28%
thirst
13%
—
patient's condition
8%
14%
fructosemia
13%
—
hypoglycemia
5%
11%
alkalization of urine
13%
—
diabetes mellitus
16%
21%
tetany
13%
—
no feeling of hunger
6%
11%
decreased potassium
13%
—
myopathy
6%
11%
drug disease
13%
—
quickly gets tired
5%
9%
lowe 's syndrome
13%
—
rapid weight loss
5%
9%
history of surgery
13%
—
loss body weight
5%
9%
wilson-konovalov disease
13%
—
diabetes mellitus in children
9%
13%
glycogenoses
12%
—
immaturity
8%
11%
vasopressin lowered
12%
—
lowered
14%
17%
hereditary amyloidosis
12%
—
weight gain
8%
11%
metabolic syndrome in children
12%
—
childhood diseases
9%
12%
nose pulmonary heart
12%
—
type 1 diabetes mellitus
8%
11%
fluid in the abdomen
12%
—
violation of the stool
7%
10%
hypotension with weakness
12%
—
dry
6%
9%
weak joints
12%
—
little urine
7%
10%
stunting
12%
—
child's poor appetite
10%
13%
thermal burns
12%
—
dependence on parents
8%
11%
decrease sodium
12%
—
appetite is poor
9%
12%
fructose intolerance
12%
—
cognitive disorders
7%
10%
parathyroid hormone increased
12%
—
no appetite
7%
10%
uremia
12%
—
hypersthenuria
11%
13%
intoxication
12%
—
diarrhea
11%
13%
little saliva
11%
—
dehydration in children
13%
15%
hypochloremia
11%
—
a history of organ transplantation
8%
10%
amyloidosis
11%
—
metabolic disorder
7%
9%
dystrophy
11%
—
blood diseases
14%
16%
mucopolysaccharidosis
11%
—
gastrointestinal problems
10%
12%
toxicosis
11%
—
increased
15%
17%
niemann-pick disease
11%
—
familial diabetes
10%
12%
chronic kidney failure
11%
—
weakness after illness
8%
9%
curvature of the legs
11%
—
dehydration
19%
20%
osteoporosis
11%
—
lags behind in the development
16%
16%
drug poisoning
11%
—
delay in physical development
11%
11%
congenital abnormalities of the ureter
11%
—
enteropathy
10%
10%
stool meager
11%
—
increased calcium
11%
—
bronchial lesion
11%
—
intestinal insufficiency syndrome
10%
—
vomiting
10%
—
impaired lung function
10%
—
obstructive uropathy
10%
—
watery feces
10%
—
chronic kidney disease
10%
—
metabolic syndrome
10%
—
increase in magnesium
10%
—
bone deformation
10%
—
heart dysfunction
10%
—
aldosterone deficiency
10%
—
in the family diabetes
10%
—
eyecardiac reflex
10%
—
hearing impaired
10%
—
vitamin d deficiency
10%
—
problems with studying
10%
—
dystrophic keratitis
10%
—
tumors of the ureter
10%
—
malabsorption
10%
—
urine does not leave
10%
—
excess aldosterone
9%
—
cancer
9%
—
diabetes insipidus in children
9%
—
pyramidal insufficiency in children
9%
—
sagging skin
9%
—
neonatal lupus
9%
—
fluid retention
9%
—
vomiting even from water
9%
—
diseases of the gastrointestinal tract
9%
—
spongy kidney
9%
—
rupture duodenal dysfunction
9%
—
primary-multiple tumors
9%
—
growth disorders in children
9%
—
decreased magnesium
9%
—
kidney transplantation
9%
—
there are no complaints
9%
—
head established magnesium deficiency
9%
—