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Comparison results

 
Results: Differences General ✘Hereditary amyloidosis✘Metachromatic leukodystrophy
Related research Analogs Analogs
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 34%—
Register, to see more distinctive signs of diseases and studies 7%32%
amyloidosis 33% —
a history of organ transplantation — 25%
worse in autumn 24% —
difficult to swallow — 24%
better in autumn 22% —
niemann-pick disease — 23%
cracking cough 21% —
progressive paralysis — 22%
antineutrophilic cytoplasmic antibodies 21% —
hepatosplenomegaly — 22%
behcet's disease 21% —
gaucher's disease — 21%
dry cough pneumonia 21% —
fabry's disease — 21%
cough dry wet 20% —
angioceratoma — 21%
amyloidosis of the kidneys 20% —
narcolepsy — 21%
Mediterranean (Marseille) fever 20% —
lags behind in the development — 20%
herpetic pneumonia 20% —
the onset of the disease during puberty — 20%
acute iritis 19% —
epilepsy attacks 6% 25%
hemophagocytic syndrome 19% —
children's speech — 19%
nephrosis 19% —
delayed motor development — 18%
nodular periarteritis 19% —
difficulty walking — 18%
hemorrhagic vasculitis 19% —
роды и вскармливание 7% 25%
juvenile rheumatoid arthritis 19% —
childhood diseases 11% 29%
polyarthritis in children 19% —
delayed speech development — 17%
pasternatsky's symptom is positive 19% —
epilepsy 6% 23%
rickettsiosis 19% —
slow onset of the disease — 17%
strong dry cough 18% —
splenectomy — 17%
acute arthritis 18% —
adynamia — 17%
bone cancer 18% —
progressive supranuclear paralysis — 17%
focal pulmonary tuberculosis 18% —
rashes dry — 17%
bone metastases 18% —
dysarthria — 17%
arterial hypertension in children 18% —
delay of mental development — 16%
joint asymmetry 18% —
cognitive disorders — 16%
the Mantoux reaction 18% —
kidney transplantation — 16%
fever abdominal pain 17% —
increased 10% 26%
croup pneumonia 17% —
epilepsy in the morning — 16%
pericarditis 17% —
hypertrophy of the left ventricle — 16%
mucus on the back wall of the pharynx 17% —
cholestasis — 16%
joint destruction 17% —
mental retardation — 15%
decrease in ESR 17% —
muscular dystonia — 15%
impaired pericardial function 17% —
leg weakness walking — 15%
epstein barr virus 17% —
affective disorders — 15%
ankylosing spondylitis 17% —
problems with studying — 15%
antinuclear antibodies 17% —
corneal opacity — 15%
with attacks of abdominal pain 17% —
muscle weakness 8% 23%
pulmonary tuberculosis 16% —
lowered 10% 25%
procalcitonin is elevated 16% —
tonic-clonic convulsions — 14%
coagulopathy 16% —
pain in the wrists — 14%
igg to herpes positive 16% —
median nerve neuropathy — 14%
Epstein-barr virus, antibodies positive 16% —
absences — 14%
viral pneumonia 16% —
weakness in the leg muscles — 14%
worse at 11 o'clock 16% —
pathological fracture — 14%
posterior rhinitis 16% —
early development — 14%
bronchopneumonia 16% —
ataxia 9% 23%
ecg voltage is too high 16% —
hears a noise — 14%
type of breathing is mixed 16% —
I can't be alone — 13%
ankylosis 16% —
speech slurred 6% 19%
hereditary angioedema 16% —
anamnesis ischemic stroke — 13%
uveit 16% —
clonic cramps — 13%
exanthema 16% —
converging strabismus — 13%
interstitial pneumonia 16% —
spleen infarction — 13%
hyperfibrinogenemia 16% —
generalized epilepsy — 13%
combined crackling 16% —
premature sexual development — 13%
interstitial lung diseases 16% —
cerebellar ataxia 7% 20%
muckle-wells syndrome 16% —
onset of illness 11% 24%
swelling of the whole body 16% —
end-stage renal failure — 13%
spondyloarthrosis 16% —
aseptic bone necrosis — 13%
polyarthritis 16% —
weakness in the legs — 13%
no cylinders 15% —
bipolar disorder — 13%
porphyria 15% —
child is not says — 13%
Epstein Barr virus antibodies 15% —
fermentopathy — 13%
gastropathy 15% —
rash on the torso — 13%
ECG voltage too low 15% —
portal hypertension — 12%
spondylopathy 15% —
blindness — 12%
weakened breathing 15% —
metabolic disorder — 12%
dry cough 15% —
twitches eyelid — 12%
chronic arthritis 15% —
tics — 12%
urticaria 15% —
infantile — 12%
periodic fever 15% —
hemarthrosis — 12%
pain in the ankles 15% —
spasm in the throat — 12%
auscultation weakened 15% —
up mania — 12%
cytomegalovirus 15% —
up imbecility — 12%
oligoarthritis 15% —
demyelinating diseases — 12%
antibodies to dna increased 15% —
laryngospasm — 12%
microhematuria 15% —
twitching of the upper eyelid — 12%
increased ldh 15% —
pseudobulbar syndrome — 12%
multiple sclerosis 15% —
cerebellar dysarthria — 12%
aortitis 15% —
juvenile absentee epilepsy — 12%
inflammation of the eyes 15% —
tinnitus — 12%
with reactive protein lowered 15% —
convulsions 10% 22%
pleurisy 15% —
constant pain — 12%
infectious arthritis 15% —
disorganization — 11%
osteosarcoma 15% —
transplant rejection reaction — 11%
severe shortness of breath 15% —
bruises do not go away for a long — 11%
breathing cough dry 15% —
severe pain in the arm — 11%
vasculitis 15% —
cold hands — 11%
pain in the joints of the fingers 15% —
liver dysfunction — 11%
daytime fever 15% —
clumsiness — 11%
muscle atrophy 15% —
enlargement of the liver and spleen 10% 21%
pain in small joints 15% —
neatness — 11%
retinitis 15% —
history of surgery 16% 27%
acute intermittent porphyria 15% —
consequences of stroke — 11%
strong cough 14% —
the lower eyelid twitches — 11%
silicotuberculosis 14% —
the feeling of falling — 11%
duration of st segment is lowered 14% —
cold wrists — 11%
bronchial lesion 14% —
liver failure — 11%

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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