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Comparison results

 
Results: Differences General ✘Hemolytic anemia✘Canavan's disease
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 100%(1)94%(25)
General blood test 54%(26)83%(17)
Coagulogram 34%(2)86%(7)
General urine test 52%(9)66%(4)
MRI of the brain —73%(0)
ECG —59%(0)
Creatinine clearance —57%(0)
Histological studies 10%(0)47%(0)
Ultrasound of the Heart 17%(0)39%(0)
Elements and vitamins 19%(5)35%(6)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 33%—
Register, to see more distinctive signs of diseases and studies —35%
hemoglobinuria 28% —
childhood diseases 7% 36%
reticulocytosis 27% —
metabolic disorder — 28%
hemolysis of erythrocytes 26% —
epilepsy attacks — 27%
taste of blood in the mouth 25% —
niemann-pick disease — 26%
paroxysmal nocturnal hemoglobinuria 24% —
epilepsy — 26%
increase ggtp 23% —
onset of illness — 25%
hemolytic anemia 21% —
convulsions — 24%
aplastic anemia 20% —
gaucher's disease — 24%
minkowski-shoffar disease 20% —
porous skin — 23%
erythropenia 18% —
wolman 's disease — 23%
prolonged fever 18% —
rashes dry — 23%
erythrocytic anemia 18% —
lags behind in the development — 22%
erythrocytosis 16% —
angioceratoma — 22%
increased indirect bilirubin 16% —
fabry's disease — 22%
increased ldh 25% 8%
narcolepsy — 22%
hemoglobinopathies 14% —
volume of spleen is increased — 22%
thalassemia 14% —
the onset of the disease during puberty — 21%
myelodysplastic syndrome 14% —
increased LDL — 21%
anemia 32% 16%
lipoidosis — 20%
hemolytic jaundice 14% —
reduction of HDL — 20%
vinegar poisoning 13% —
alt reduction — 20%
sickle cell anemia 12% —
neurological disorders — 20%
hypochromia 12% —
increased HDL — 20%
chronic monocytic leukemia 12% —
history of surgery 11% 31%
iron deficiency anemia 12% —
muscle weakness — 20%
bilirubinuria 12% —
slowness of movement — 19%
arsenic poisoning 11% —
familial endogenous hypertriglyceridemia — 19%
dyspnea 11% —
liver transplantation — 19%
tonsillitis in leukemia 11% —
congenital liver fibrosis — 19%
portal vein thrombosis 11% —
macrocephaly — 19%
immune hemolytic anemia 10% —
increased cholesterol levels in the blood — 19%
weakness and palpitations 10% —
reduction of ast — 19%
calculous cholecystitis gallbladder stones 10% —
difficult to swallow 7% 26%
brown feces 10% —
reduction of LDL — 19%
intestinal lymphoma 10% —
malabsorption — 18%
budd—chiari syndrome 10% —
unformed feces — 18%
acute calculous cholecystitis 10% —
hearing impaired — 18%
tingling in the side 9% —
primary hypercholesterolemia — 18%
calculous cholecystitis 9% —
impaired spleen function — 18%
palpitations with shortness of breath 9% —
liver failure — 18%
acute venous thrombosis 9% —
dry — 18%
polydactyly 9% —
enteropathy — 18%
hyperbilirubinemia 24% 13%
history of liver surgery — 18%
secondary syphilis 9% —
increased ast — 18%
acute lymphoblastic leukemia 9% —
progressive supranuclear paralysis — 18%
hyperphosphatemia 9% —
hepatosplenomegaly 9% 27%
transferrin increase 9% —
diarrhea — 18%
enzymatic insufficiency 9% —
hypotension with weakness — 18%
crystalluria 9% —
lower cholesterol — 18%
lesion increased 9% —
hepatosis — 17%
basophilia 9% —
rupture duodenal dysfunction — 17%
weakness when breathing 9% —
cognitive disorders — 17%
palpitations 17% 6%
hypertrophy of the left ventricle — 17%
consequences of vaccinations 9% —
intestinal insufficiency syndrome — 17%
acute leukemia 8% —
hepatosis fatty — 17%
purulent sore throats 8% —
epilepsy in the morning — 17%
lymphocytic 8% —
adynamia — 17%
general weakness 8% —
cholesterolemia — 17%
anuria 8% —
liver dysfunction — 17%
rhesus conflict 8% —
expansion of the esophagus — 17%
vascular tumor 8% —
increased alt — 17%
vitamin b12 reduction2 8% —
sluggish baby — 17%
malocclusion 8% —
hyperlipidemia — 17%
biliary colic 8% —
patient's condition 5% 22%
post-traumatic shock 8% —
violation of the stool — 16%
anemia in children 8% —
calcification — 16%
black feces 8% —
enlargement of the liver and spleen 11% 27%
hemolytic disease of newborns 8% —
hypotension — 16%
lymphogranulomatosis 8% —
impaired lung function — 16%
curvature of the nose 8% —
liver problems 5% 21%
thrombocytopenic purpura 8% —
ataxia — 16%
infectious mononucleosis 8% —
early development — 16%
porphyria 8% —
affective disorders — 16%
cylindruria 8% —
kidney transplantation — 16%
decrease in ESR 8% —
effects of puberty — 16%
chronic lymphocytic 8% —
liver atrophy — 16%
black discharge 8% —
polyneuropathy — 16%
gothic sky 8% —
dyslipidemia — 16%
decreased vitamin b9 8% —
need for fats — 16%
postvaccinal reaction 8% —
corneal opacity — 16%
malignant arterial hypertension 8% —
infantile — 16%
mononucleosis 8% —
hypotension — 16%
rectal cancer 8% —
blindness — 16%
malaria 8% —
arrhythmia — 16%
malignant lymphoma 7% —
delirium — 15%
mch increased 7% —
limbs pain — 15%
monocytopenia 7% —
hemophagocytic syndrome — 15%
toxoplasmosis 7% —
increased bleeding — 15%
bone growths 7% —
anomalies of esophageal development — 15%
microcytic anemia 7% —
memory impairment — 15%
shortness of breath attacks 7% —
swelling — 15%
increased potassium 7% —
neurogenic pain — 15%
gallbladder stones 7% —
confusion of consciousness — 15%
cholecystitis 7% —
2 children — 15%
increased serum iron 7% —
nose nursing mom — 15%
dic syndrome 7% —
up circulatory disorders — 15%
kidney damage 7% —
damage to the nervous system 3% 18%
colic 7% —
heart hypertrophy — 15%
heart murmurs 7% —
abdominal pain after diarrhea — 15%
myelofibrosis 7% —
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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