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Comparison results

 
Results: Differences General ✘Dubin-Johnson syndrome✘Canavan's disease
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 100%(4)94%(25)
General blood test 32%(2)83%(17)
Coagulogram 19%(1)86%(7)
General urine test 26%(6)66%(4)
MRI of the brain —73%(0)
ECG —59%(0)
Creatinine clearance —57%(0)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 32%—
Register, to see more distinctive signs of diseases and studies —36%
leukocyturia 26% —
canavan's disease — 35%
rotor syndrome 24% —
history of surgery — 31%
increased indirect bilirubin 16% —
metabolic disorder — 28%
chronic cholangitis 12% —
epilepsy attacks — 27%
bilirubinuria 11% —
enlargement of the liver and spleen — 27%
no gallbladder 11% —
hepatosplenomegaly — 27%
dark urine 11% —
niemann-pick disease — 26%
yellow skin color 11% —
enlargement of the spleen — 26%
cholangitis 10% —
difficult to swallow — 26%
nausea from fatigue 10% —
epilepsy — 26%
itching of the skin of the abdomen 10% —
onset of illness — 25%
congestion belching 8% —
lowered 6% 30%
toxic liver 8% —
convulsions — 24%
dysfunction of the gallbladder 8% —
enlarged liver — 24%
deterioration during pregnancy 8% —
gaucher's disease — 24%
proteinuria 23% 14%
rashes dry — 23%
jaundice 17% 13%
porous skin — 23%
hyperbilirubinemia 17% 13%
wolman 's disease — 23%
narcolepsy — 22%
angioceratoma — 22%
fabry's disease — 22%
lags behind in the development — 22%
volume of spleen is increased — 22%
hypersplenism — 21%
consequences of taking medications — 21%
portal hypertension — 21%
increased LDL — 21%
the onset of the disease during puberty — 21%
increased 11% 32%
increased HDL — 20%
muscle weakness — 20%
heart dysfunction — 20%
hypertension — 20%
alt reduction — 20%
neurological disorders — 20%
reduction of HDL — 20%
lipoidosis — 20%
increased cholesterol levels in the blood — 19%
familial endogenous hypertriglyceridemia — 19%
reduction of ast — 19%
diseases of the gastrointestinal tract — 19%
macrocephaly — 19%
a history of organ transplantation — 19%
blood diseases — 19%
congenital liver fibrosis — 19%
slowness of movement — 19%
liver transplantation — 19%
cholestasis — 19%
reduction of LDL — 19%
impaired arterial function — 19%
enteropathy — 18%
hearing impaired — 18%
heart failure — 18%
gastrointestinal problems — 18%
liver failure — 18%
malabsorption — 18%
unformed feces — 18%
primary hypercholesterolemia — 18%
damage to the nervous system — 18%
increased ast — 18%
impaired venous function — 18%
thrombocytopenia — 18%
hypotension with weakness — 18%
there is heart failure — 18%
impaired spleen function — 18%
history of liver surgery — 18%
lower cholesterol — 18%
splenectomy — 18%
progressive supranuclear paralysis — 18%
diarrhea — 18%
dry — 18%
leukopenia — 17%
congenital anomalies of the lower extremities — 17%
cognitive disorders — 17%
hepatosis — 17%
paranoia — 17%
hyperlipidemia — 17%
cholesterolemia — 17%
hepatosis fatty — 17%
adynamia — 17%
there are no complaints — 17%
high temperature — 17%
control issues — 17%
increased alt — 17%
sluggish baby — 17%
cardiac cirrhosis of the liver — 17%
rupture duodenal dysfunction — 17%
hemorrhagic diathesis — 17%
intestinal insufficiency syndrome — 17%
hypertrophy of the left ventricle — 17%
expansion of the esophagus — 17%
hypotension — 16%
anemia — 16%
hypotension — 16%
calcification — 16%
chronic venous edema — 16%
ascites — 16%
cirrhosis of the liver — 16%
general swelling does — 16%
ataxia — 16%
swelling of the legs — 16%
periodic illness — 16%
polyneuropathy — 16%
arrhythmia — 16%
need for fats — 16%
muscular dystonia — 16%
angiopathy — 16%
impaired lung function — 16%
kidney transplantation — 16%
blindness — 16%
stroke — 16%
affective disorders — 16%
drug disease 6% 22%
CHD — 16%
early development — 16%
chronic heart failure — 16%
suspicion — 16%
corneal opacity — 16%
violation of the stool — 16%
infantile — 16%
effects of puberty — 16%
epilepsy in the morning — 16%
dyslipidemia — 16%
liver atrophy — 16%
patient's condition 6% 22%
anomalies of esophageal development — 15%
chronic kidney failure — 15%
up circulatory disorders — 15%
memory impairment — 15%
limbs pain — 15%
necrosis — 15%
neurogenic pain — 15%
joint diseases — 15%
impaired coordination — 15%
2 children — 15%
abdominal swelling — 15%
increased bleeding — 15%
hemophagocytic syndrome — 15%
heart hypertrophy — 15%
delirium — 15%
impaired kidney function — 15%
nose nursing mom — 15%
angioplasty — 15%
venous congestion — 15%
swelling — 15%
confusion of consciousness — 15%
abdominal pain after diarrhea — 15%
steatorrhea — 15%
madness — 15%
pathological fracture — 15%
neurological pain — 15%
fever intermittent — 14%
diarrhea in the morning — 14%
paralysis — 14%
children's speech — 14%
spleen infarction — 14%
converging strabismus — 14%
tonic-clonic convulsions — 14%
median nerve neuropathy — 14%
end-stage renal failure — 14%
vomiting — 14%
cerebral circulation disorder — 14%
I can't be alone — 14%
generalized epilepsy — 14%
abundant stool — 14%
cataract — 14%
optimistic — 14%
stool with gases — 14%
ophthalmoplegia — 14%
varicose veins of the esophagus — 14%
absences — 14%
kidney failure — 14%
forgetfulness — 14%
роды и вскармливание 6% 20%
clonic cramps — 14%
bipolar disorder — 14%
congestive kidney — 14%
a difficult teenager — 14%
atherosclerosis of blood vessels — 14%
progressive paralysis — 14%
premature sexual development — 14%
bloating — 14%

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.
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