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Comparison results

 
Results: Differences General ✘Hereditary amyloidosis✘Canavan's disease
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 100%(20)94%(25)
Coagulogram 89%(16)86%(7)
General blood test 68%(23)83%(17)
General urine test 61%(18)66%(4)
ECG 37%(0)59%(0)
MRI of the brain 8%(0)73%(0)
Creatinine clearance 15%(0)57%(0)
Histological studies 18%(0)47%(0)
Ultrasound of the Heart 13%(0)39%(0)
Autoimmune markers 21%(8)29%(2)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 34%—
Register, to see more distinctive signs of diseases and studies —35%
amyloidosis 33% —
metabolic disorder — 28%
worse in autumn 24% —
hepatosplenomegaly — 27%
better in autumn 22% —
difficult to swallow — 26%
behcet's disease 21% —
niemann-pick disease — 26%
antineutrophilic cytoplasmic antibodies 21% —
childhood diseases 11% 36%
cracking cough 21% —
gaucher's disease — 24%
dry cough pneumonia 21% —
rashes dry — 23%
cough dry wet 20% —
porous skin — 23%
herpetic pneumonia 20% —
wolman 's disease — 23%
Mediterranean (Marseille) fever 20% —
angioceratoma — 22%
amyloidosis of the kidneys 20% —
fabry's disease — 22%
juvenile rheumatoid arthritis 19% —
lags behind in the development — 22%
nodular periarteritis 19% —
narcolepsy — 22%
nephrosis 19% —
increased 10% 32%
hemorrhagic vasculitis 19% —
the onset of the disease during puberty — 21%
polyarthritis in children 19% —
portal hypertension — 21%
rickettsiosis 19% —
epilepsy attacks 6% 27%
acute iritis 19% —
increased LDL — 21%
bone cancer 18% —
hypersplenism — 21%
joint asymmetry 18% —
increased HDL — 20%
strong dry cough 18% —
alt reduction — 20%
arterial hypertension in children 18% —
reduction of HDL — 20%
bone metastases 18% —
lowered 10% 30%
focal pulmonary tuberculosis 18% —
epilepsy 6% 26%
pasternatsky's symptom is positive 18% —
a history of organ transplantation — 19%
acute arthritis 18% —
macrocephaly — 19%
the Mantoux reaction 18% —
cholestasis — 19%
mucus on the back wall of the pharynx 17% —
slowness of movement — 19%
joint destruction 17% —
congenital liver fibrosis — 19%
croup pneumonia 17% —
increased cholesterol levels in the blood — 19%
with attacks of abdominal pain 17% —
liver transplantation — 19%
impaired pericardial function 17% —
reduction of LDL — 19%
antinuclear antibodies 17% —
familial endogenous hypertriglyceridemia — 19%
decrease in ESR 17% —
reduction of ast — 19%
fever abdominal pain 17% —
liver failure — 18%
ankylosing spondylitis 17% —
hypotension with weakness — 18%
epstein barr virus 17% —
primary hypercholesterolemia — 18%
ecg voltage is too high 16% —
history of liver surgery — 18%
viral pneumonia 16% —
splenectomy — 18%
bronchopneumonia 16% —
progressive supranuclear paralysis — 18%
posterior rhinitis 16% —
epilepsy in the morning — 17%
procalcitonin is elevated 16% —
cognitive disorders — 17%
coagulopathy 16% —
expansion of the esophagus — 17%
combined crackling 16% —
sluggish baby — 17%
igg to herpes positive 16% —
hypertrophy of the left ventricle — 17%
hereditary angioedema 16% —
liver dysfunction — 17%
uveit 16% —
hepatosis fatty — 17%
polyarthritis 16% —
congenital anomalies of the lower extremities — 17%
interstitial pneumonia 16% —
cardiac cirrhosis of the liver — 17%
ankylosis 16% —
adynamia — 17%
spondyloarthrosis 16% —
hepatosis — 17%
interstitial lung diseases 16% —
enlargement of the liver and spleen 10% 27%
swelling of the whole body 16% —
muscular dystonia — 16%
pericarditis 16% —
affective disorders — 16%
exanthema 16% —
calcification — 16%
hyperfibrinogenemia 16% —
early development — 16%
Epstein-barr virus, antibodies positive 16% —
kidney transplantation — 16%
worse at 11 o'clock 16% —
chronic venous edema — 16%
muckle-wells syndrome 16% —
liver atrophy — 16%
Epstein Barr virus antibodies 15% —
dyslipidemia — 16%
ECG voltage too low 15% —
cirrhosis of the liver — 16%
spondylopathy 15% —
blindness — 16%
type of breathing is mixed 15% —
infantile — 16%
antibodies to dna increased 15% —
corneal opacity — 16%
no cylinders 15% —
hypotension — 16%
periodic fever 15% —
pathological fracture — 15%
cytomegalovirus 15% —
history of surgery 16% 31%
pain in the ankles 15% —
anomalies of esophageal development — 15%
auscultation weakened 15% —
nose nursing mom — 15%
chronic arthritis 15% —
steatorrhea — 15%
microhematuria 15% —
progressive paralysis — 14%
inflammation of the eyes 15% —
clonic cramps — 14%
acute intermittent porphyria 15% —
premature sexual development — 14%
pain in small joints 15% —
absences — 14%
oligoarthritis 15% —
fever intermittent — 14%
multiple sclerosis 15% —
cytolysis syndrome — 14%
retinitis 15% —
pain in the wrists — 14%
pain in the joints of the fingers 15% —
chills in the afternoon — 14%
with reactive protein lowered 15% —
bipolar disorder — 14%
pulmonary tuberculosis 15% —
optimistic — 14%
aortitis 15% —
generalized epilepsy — 14%
porphyria 15% —
I can't be alone — 14%
vasculitis 15% —
atherosclerosis of blood vessels — 14%
daytime fever 15% —
varicose veins of the esophagus — 14%
weakened breathing 15% —
children's speech — 14%
gastropathy 15% —
onset of illness 11% 25%
breathing cough dry 15% —
converging strabismus — 14%
infectious arthritis 15% —
diarrhea in the morning — 14%
osteosarcoma 15% —
tonic-clonic convulsions — 14%
severe shortness of breath 15% —
median nerve neuropathy — 14%
bronchial lesion 14% —
spleen infarction — 14%
silicotuberculosis 14% —
hears a noise — 14%
asleep leg muscle pain 14% —
convulsions 10% 24%
intestinal obstruction 14% —
end-stage renal failure — 14%
duration of st segment is lowered 14% —
juvenile absentee epilepsy — 13%
loose stools with mucus 14% —
demyelinating diseases — 13%
metastases 14% —
meteorism in the morning — 13%
pulmonary mycoplasmosis 14% —
little fat in the fecal — 13%
respiratory insufficiency 14% —
stool in the morning — 13%
strong cough 14% —
behavioral disorders in children — 13%

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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