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Comparison results

 
Results: Differences General ✘Lipoid nephrosis✘Canavan's disease
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 100%(7)94%(25)
General blood test 53%(17)83%(17)
Coagulogram 48%(7)86%(7)
General urine test 66%(17)66%(4)
ECG 46%(0)59%(0)
MRI of the brain —73%(0)
Creatinine clearance 11%(0)57%(0)
Histological studies 16%(0)47%(0)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 36%—
Register, to see more distinctive signs of diseases and studies —35%
lipoid nephrosis 33% —
metabolic disorder — 28%
nephrosis 29% —
hepatosplenomegaly — 27%
nephrotic syndrome 40% 9%
enlargement of the liver and spleen — 27%
hypoproteinemia 28% —
epilepsy attacks — 27%
changes in urine 22% —
niemann-pick disease — 26%
berger 's disease 22% —
difficult to swallow — 26%
acute glomerulonephritis 21% —
enlargement of the spleen — 26%
hereditary jade 21% —
epilepsy — 26%
little urine 21% —
onset of illness — 25%
inflammation of the kidneys 29% 7%
gaucher's disease — 24%
facial swelling 20% —
convulsions — 24%
hematuric nephritis 19% —
wolman 's disease — 23%
desire for warm water 19% —
porous skin — 23%
microhematuria 19% —
rashes dry — 23%
alport syndrome 19% —
volume of spleen is increased — 22%
kidney failure in children 18% —
lags behind in the development — 22%
crystalluria 18% —
narcolepsy — 22%
hematuria 25% 6%
angioceratoma — 22%
leukocyturia 17% —
fabry's disease — 22%
nephrosclerosis 17% —
increased LDL — 21%
proteinuria 33% 14%
portal hypertension — 21%
oliguria 17% —
the onset of the disease during puberty — 21%
swelling of eyelids 16% —
hypersplenism — 21%
malaria 16% —
alt reduction — 20%
antinuclear factor 16% —
reduction of HDL — 20%
eating ice 16% —
muscle weakness — 20%
antineutrophilic cytoplasmic antibodies 16% —
роды и вскармливание — 20%
anasarka 16% —
lipoidosis — 20%
mercury poisoning 15% —
increased HDL — 20%
pale puffy face 15% —
neurological disorders — 20%
rapidly progressive glomerulonephritis 15% —
reduction of ast — 19%
glomerulonephritis in children 15% —
macrocephaly — 19%
uremia 15% —
a history of organ transplantation — 19%
oily facial skin 15% —
congenital liver fibrosis — 19%
swelling of the face in the morning 14% —
liver transplantation — 19%
nephropathy 28% 12%
familial endogenous hypertriglyceridemia — 19%
white blood cells and red blood cells in the urine 14% —
slowness of movement — 19%
chronic dysentery 14% —
cholestasis — 19%
puffiness of the eyelids in the morning 14% —
reduction of LDL — 19%
subcutaneous edema 14% —
unformed feces — 18%
violation of protein metabolism 14% —
splenectomy — 18%
intestinal lymphoma 14% —
hypotension with weakness — 18%
glomerulonephritis 24% 8%
diarrhea — 18%
thirst 13% —
increased ast — 18%
tuberculosis intoxication 13% —
progressive supranuclear paralysis — 18%
no discharge 13% —
malabsorption — 18%
antithrombin is elevated 13% —
liver failure — 18%
urine light 13% —
damage to the nervous system — 18%
brown urine 13% —
lower cholesterol — 18%
altitude sickness 13% —
history of liver surgery — 18%
chronic arthritis 13% —
dry — 18%
bacterial dysentery 13% —
primary hypercholesterolemia — 18%
is very sensitive 13% —
enteropathy — 18%
systemic lupus erythematosus 12% —
impaired spleen function — 18%
kidney damage 12% —
impaired venous function — 18%
cylindruria 12% —
hypertrophy of the left ventricle — 17%
aslo is reduced 12% —
liver dysfunction — 17%
lead poisoning 12% —
congenital anomalies of the lower extremities — 17%
syphilis 12% —
hemorrhagic diathesis — 17%
tuberculosis arthritis 12% —
hepatosis fatty — 17%
azotemia 12% —
increased alt — 17%
amyloidosis of the kidneys 12% —
cardiac cirrhosis of the liver — 17%
pulmonary edema 12% —
adynamia — 17%
dysentery 12% —
hepatosis — 17%
chronic enterocolitis 12% —
cognitive disorders — 17%
hypogammaglobulinemia 12% —
paranoia — 17%
sediment urine 22% 8%
sluggish baby — 17%
lymphogranulomatosis 11% —
expansion of the esophagus — 17%
liebman-sachs endocarditis 11% —
corneal opacity — 16%
hypersthenuria 11% —
liver atrophy — 16%
diphtheria 11% —
hypotension — 16%
pale face 11% —
CHD — 16%
chronic osteomyelitis 11% —
polyneuropathy — 16%
independent child 11% —
kidney transplantation — 16%
intestinal colic 11% —
chronic venous edema — 16%
tuberculosis of bones 11% —
hypertrophy biliary tract — 16%
very pale 11% —
calcification — 16%
the heart tones are muted 11% —
cirrhosis of the liver — 16%
hemorrhagic syndrome 11% —
abdominal pain — 16%
chilly 11% —
general swelling does — 16%
multiple kidney stones 11% —
ataxia — 16%
tuberculosis of the joints 11% —
dyslipidemia — 16%
enterocolitis 11% —
angiopathy — 16%
endocarditis 11% —
stroke — 16%
hypochromia 10% —
need for fats — 16%
syphilis in children 10% —
early development — 16%
impaired kidney function 27% 15%
violation of the stool — 16%
the surface is smooth 10% —
impaired lung function — 16%
duodenitis 10% —
enlarged liver 8% 24%
blisters 10% —
arrhythmia — 16%
colic 10% —
chronic heart failure — 16%
secondary syphilis 10% —
suspicion — 16%
iron deficiency anemia 10% —
muscular dystonia — 16%
decrease in creatinine 10% —
affective disorders — 16%
infectious colitis 10% —
swelling of the legs — 16%
viral endocarditis 10% —
blindness — 16%
polyarthritis 10% —
effects of puberty — 16%
nephritic syndrome 10% —
infantile — 16%
immunoglobulin a deficiency 10% —
epilepsy in the morning — 16%
oxalaturia 10% —
steatorrhea — 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.
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