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Comparison results

 
Results: Differences General ✘Nephronophthys Fanconi✘Canavan's disease
Related research Analogs Analogs
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 100%—
Register, to see more distinctive signs of diseases and studies —35%
joubert syndrome 89% —
metabolic disorder — 28%
rickets -like diseases 71% —
epilepsy attacks — 27%
polyuria 67% —
hepatosplenomegaly — 27%
azotemia 64% —
enlargement of the liver and spleen — 27%
iron deficiency anemia 63% —
epilepsy — 26%
hypochromia 63% —
enlargement of the spleen — 26%
frequent urination at night 57% —
niemann-pick disease — 26%
isolates himself 55% —
difficult to swallow — 26%
fanconi anemia 53% —
gaucher's disease — 24%
speeded up urination 50% —
enlarged liver — 24%
hematuria 58% 6%
wolman 's disease — 23%
decreased calcium 49% —
rashes dry — 23%
thirst 49% —
porous skin — 23%
no thirst 48% —
drug disease — 22%
hypostenuria 47% —
narcolepsy — 22%
anemia 63% 16%
volume of spleen is increased — 22%
impaired kidney function 62% 15%
angioceratoma — 22%
kidney failure 61% 14%
fabry's disease — 22%
drinks a lot of fluids 45% —
consequences of taking medications — 21%
hypophosphatemia 44% —
increased LDL — 21%
nocturnal diuresis 43% —
the onset of the disease during puberty — 21%
microhematuria 43% —
portal hypertension — 21%
renal anemia 42% —
liver problems — 21%
hypersthenuria 40% —
hypersplenism — 21%
tonic convulsions 40% —
increased HDL — 20%
hyperparathyroidism 39% —
heart dysfunction — 20%
kidney transplantation 57% 16%
lipoidosis — 20%
prolonged urination 39% —
reduction of HDL — 20%
anomalies of kidney development 38% —
muscle weakness — 20%
chronic anemia 47% 7%
alt reduction — 20%
kidney cyst 38% —
neurological disorders — 20%
frequent dizziness 37% —
роды и вскармливание — 20%
convulsive syndrome in children 37% —
hypertension — 20%
terminal states 36% —
macrocephaly — 19%
changes in urine 36% —
liver transplantation — 19%
variable symptoms 33% —
diseases of the gastrointestinal tract — 19%
chronic kidney failure 47% 15%
blood diseases — 19%
cysts 29% —
congenital liver fibrosis — 19%
proteinuria 45% 14%
familial endogenous hypertriglyceridemia — 19%
convulsions in the anamnesis 40% 11%
reduction of ast — 19%
cramps in the legs 33% 7%
slowness of movement — 19%
delay in physical development 35% 10%
cholestasis — 19%
convulsions 49% 24%
impaired arterial function — 19%
tachycardia 29% 6%
increased cholesterol levels in the blood — 19%
a history of organ transplantation 42% 19%
reduction of LDL — 19%
changes in the blood 29% 6%
thrombocytopenia — 18%
sepsis 29% 6%
enteropathy — 18%
palpitations 28% 6%
damage to the nervous system — 18%
helps others 28% 6%
hypotension with weakness — 18%
dizziness 30% 10%
unformed feces — 18%
not enough time 29% 10%
hearing impaired — 18%
nephropathy 31% 12%
gastrointestinal problems — 18%
protein with increased 30% 12%
malabsorption — 18%
hypotension 33% 16%
lower cholesterol — 18%
congestive kidney 31% 14%
primary hypercholesterolemia — 18%
I can't be alone 30% 14%
impaired venous function — 18%
imbalance 27% 12%
increased ast — 18%
madness 30% 15%
heart failure — 18%
delirium 30% 15%
dry — 18%
confusion of consciousness 29% 15%
impaired spleen function — 18%
oncology 24% 10%
history of liver surgery — 18%
hypotension 29% 16%
there is heart failure — 18%
onset of illness 36% 25%
splenectomy — 18%
lags behind in the development 28% 22%
progressive supranuclear paralysis — 18%
diarrhea — 18%
liver failure — 18%
increased alt — 17%
paranoia — 17%
adynamia — 17%
there are no complaints — 17%
cholesterolemia — 17%
expansion of the esophagus — 17%
cardiac cirrhosis of the liver — 17%
sluggish baby — 17%
hypertrophy of the left ventricle — 17%
hemorrhagic diathesis — 17%
control issues — 17%
epilepsy in the morning — 17%
high temperature — 17%
cognitive disorders — 17%
rupture duodenal dysfunction — 17%
hepatosis — 17%
hepatosis fatty — 17%
intestinal insufficiency syndrome — 17%
congenital anomalies of the lower extremities — 17%
hyperlipidemia — 17%
leukopenia — 17%
liver dysfunction — 17%
chronic heart failure — 16%
arrhythmia — 16%
blindness — 16%
affective disorders — 16%
periodic illness — 16%
suspicion — 16%
polyneuropathy — 16%
corneal opacity — 16%
swelling of the legs — 16%
violation of the stool — 16%
hypertrophy biliary tract — 16%
CHD — 16%
muscular dystonia — 16%
impaired lung function — 16%
infantile — 16%
chronic venous edema — 16%
ataxia — 16%
angiopathy — 16%
need for fats — 16%
cirrhosis of the liver — 16%
quickly gets tired — 16%
calcification — 16%
early development — 16%
ascites — 16%
general swelling does — 16%
stroke — 16%
effects of puberty — 16%
liver atrophy — 16%
dyslipidemia — 16%
abdominal pain — 16%
heart hypertrophy — 15%
neurogenic pain — 15%
necrosis — 15%
up circulatory disorders — 15%
anomalies of esophageal development — 15%
impaired coordination — 15%
2 children — 15%
joint diseases — 15%
memory impairment — 15%
limbs pain — 15%
abdominal swelling — 15%
hemophagocytic syndrome — 15%
abdominal pain after diarrhea — 15%
nose nursing mom — 15%
steatorrhea — 15%
pathological fracture — 15%
neurological pain — 15%
venous congestion — 15%

Instructions

Video
  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.
  6. By using the service, you agree to user agreement. Kiberis services do not replace a doctor!
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