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Comparison results

 
Results: Differences General ✘Bartter syndrome✘Phenylketonuria
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 99%(4)28%(5)
Blood biochemistry 10%(1)100%(1)
General urine test 15%(5)94%(7)
General blood test 13%(1)75%(3)
Autoimmune markers 66%(1)15%(1)
ECG —71%(0)
MRI of the brain —51%(0)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 32%—
Register, to see more distinctive signs of diseases and studies 11%69%
metabolic alkalosis 25% —
mental retardation — 56%
polyuria 24% —
phenylketonuria — 49%
renin lowered 24% —
delayed speech development 13% 56%
alkalosis 23% —
children's speech 12% 54%
decreased potassium 22% —
nocturnal enuresis — 39%
hyperphosphatemia 19% —
foolishness — 37%
hypomagnesemia 19% —
childish behavior — 37%
head established magnesium deficiency 19% —
nervous excitability — 37%
dehydration in children 18% —
increased 6% 43%
dehydration 17% —
often sick child — 36%
feeling of stiffness in the chest 17% —
microcephaly — 35%
hyperaldosteronism 16% —
infantile — 35%
calcium in urine is elevated 15% —
urinary incontinence — 34%
secondary hyperaldosteronism 14% —
fontanelle — 33%
feeling of cramps 14% —
childhood diseases 12% 43%
loss body weight 14% —
short height — 31%
tendency to constipation 14% —
speech slurred — 30%
hypertensive dehydration 14% —
muscular dystonia — 29%
renin increased 14% —
frequent colds — 28%
hypotension with weakness 14% —
immunodeficiency — 28%
rapid weight loss 14% —
emotional — 28%
hypostenuria 13% —
mental all — 28%
tingling in the chest 13% —
fidgety — 26%
feeling of weakness in the heart 13% —
overexcitation of the psyche — 26%
tetany 13% —
dysmetabolic nephropathy — 26%
tingling in the heart area 13% —
segawa syndrome — 25%
urination is regular 13% —
skin problems — 25%
hypotonic dehydration 12% —
anemia — 25%
tingling in the body 12% —
2 children — 25%
adrenal hyperplasia 12% —
epilepsy — 25%
arterial hypertension in children 12% —
eczema — 24%
stiffness in the body 12% —
eats inedible — 24%
polyhydramnios during pregnancy 12% —
blood serotonin is lowered — 23%
drinks a lot of fluids 12% —
onset of illness — 23%
thirst is reduced 12% —
hyperkinesis in children — 23%
severe childbirth 11% —
high intelligence — 23%
tingling in the extremities 11% —
light hair — 23%
hypertension 11% —
teething later — 22%
cyclic vomiting 11% —
body odor — 22%
feeling of stiffness 11% —
tremor — 22%
familial hypertension 11% —
idiocy — 22%
prolonged urination 11% —
smell of sweat unpleasant — 22%
fatigue in the morning 11% —
paresis of the hand — 22%
loss of strength in the morning 11% —
lowered 15% 37%
speaks poorly 11% —
up imbecility — 21%
child's poor appetite 11% —
patient's condition — 21%
listlessness drowsiness 11% —
absences — 21%
urination with blood 11% —
hyperkinesis — 21%
hypersthenuria 11% —
fetid urine — 21%
weakness in the heart 10% —
heart defect — 21%
premature birth 10% —
liver problems — 21%
no discharge 10% —
high height — 21%
weakness in the extremities 10% —
belching from milk — 20%
vomiting with blood 10% —
history medical mother's — 20%
he feels his heart 10% —
wound — 20%
thirst 10% —
nose nursing mom — 20%
feeling of crawling goosebumps 10% —
hyperactive — 20%
adrenal insufficiency 10% —
crystalluria — 20%
vomiting even from water 10% —
tetraparesis — 20%
eats 10% —
tonic-clonic convulsions — 19%
weak heart 10% —
clonic cramps — 19%
increased potassium 10% —
generalized epilepsy — 19%
loss of work 10% —
bright eyes — 19%
is gaining weight poorly 10% —
epilepsy attacks — 19%
muscle fatigue 10% —
improvement after sleep — 19%
increased calcium 10% —
paresis of legs — 18%
weight gain 9% —
heart defects in pregnant women — 18%
electrolyte balance disorders 9% —
dependence on food — 18%
tingling 9% —
paresis — 18%
sensations in the extremities 9% —
teething the child — 18%
quickly gets tired 8% —
dermatitis and eczema — 18%
chronic condition 8% —
1 pregnancy — 18%
essential hypertension 8% —
muscular dystonia in a child — 18%
visual impairment 8% —
convulsive syndrome in children — 18%
imbalance 8% —
tremor of the hands — 18%
early development 8% —
weakness after sleep — 17%
rapid reaction 8% —
consultation of a gastroenterologist — 17%
weakness after illness 15% 9%
diseases of the gastrointestinal tract — 17%
sluggish baby 17% 12%
body odor unpleasant — 17%
stunting 13% 8%
eczema peeling — 17%
muscle weakness 18% 14%
galactosemia — 17%
problems with studying — 17%
shaky gait — 17%
pylorostenosis — 17%
spasm — 17%
children's aphasia — 17%
consultation with a cardiologist — 17%
cramps of the hands — 16%
convulsions 11% 27%
trembling in the legs — 16%
worse when walking — 16%
delayed motor development — 16%
sweaty baby — 16%
cognitive disorders 9% 25%
oncology — 16%
psychologist — 16%
hypothyroidism in children — 15%
pain in the left hypochondrium — 15%
decreased vitamin b9 — 15%
angioplasty — 15%
tremor in the legs — 15%
better after a nap — 15%
fair skin — 15%
selenium deficiency — 15%
liver failure — 15%
somatoform dysfunction of the autonomic nervous system — 15%
liver dysfunction — 15%
hypoplasia of enamel — 15%
tracheopesophageal fistula — 15%
worse in violation of the diet — 15%
renal osteodystrophy — 15%
osteoporosis — 15%
роды и вскармливание 7% 22%
intrauterine fetal development delay — 14%
dermatitis — 14%
constipation children — 14%
blonde with blue eyes — 14%
sweating is increased — 14%
congenital hypothyroidism — 14%

Instructions

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  1. Introduce new diseases through 🔍 Search and input on the top panel using
  2. The table shows the most important distinguishing symptoms, tests and diagnoses related to the selected diseases.
  3. The higher the percentage, the more important this symptom is for the disease and vice versa. At 0%, we can say that this symptom never occurs in the disease.
  4. The list changes dynamically depending on the data of the current visit in the selection of therapy .
  5. Click on the percentageto see the suggestions from the original source.
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