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Comparison results

 
Results: Differences Similar Metachromatic leukodystrophyJoubert syndrome
Related research Analogs Analogs
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 29%
Register, to see more distinctive signs of diseases and studies 100%
niemann-pick disease 29%
encephalocele 57%
progressive paralysis 27%
polycystic liver 48%
cataplexy 26%
coloboma 46%
angioceratoma 26%
rapid breathing 40%
fabry's disease 26%
liver cysts 40%
another refined dermatitis 26%
kidney cyst 37%
epilepsy attacks 26%
macular 37%
difficult to swallow 26%
polycystic 35%
the onset of the disease during puberty 26%
hydrocephalus 34%
epilepsy 25%
cystic fibrosis 33%
paralysis 24%
bradypnea 32%
damage to the nervous system 23%
idiocy 32%
convulsions 23%
akathisia 32%
onset of illness 23%
brain development abnormalities 31%
difficulty walking 22%
ataxia in children 31%
hypertension 22%
polycystic kidney 30%
slow onset of the disease 21%
cochlear neuritis 29%
consequences of taking medications 21%
breath retention 28%
rashes dry 21%
better from movement 28%
weakness 20%
involuntary movements 28%
dysarthria 20%
change of teeth 27%
cholestasis 20%
hearing loss in children 27%
progressive supranuclear paralysis 20%
intellectual disabilities in children 8% 35%
hypertrophy of the left ventricle 20%
weakness of the eyes 26%
delayed speech development 19%
weak breathing 26%
polyneuropathy 19%
anomalies of kidney development 26%
effects of puberty 19%
apnea 8% 34%
loss of balance 19%
smart baby 8% 33%
heart hypertrophy 19%
big head 25%
neurogenic pain 18%
sluggish baby 8% 33%
epilepsy in children 18%
nystagmus 25%
memory 18%
deafness 24%
early development 18%
weakness when breathing 24%
enlargement of the spleen 18%
cirrhosis of the liver 8% 32%
2 children 18%
inflammation of the eyes 23%
corneal 18%
growth disorders in children 23%
emotional 18%
neuritis 23%
leg weakness walking 18%
eye surgery 22%
affective disorders 18%
weakness after illness 15% 37%
dystonia 18%
neuralgia 22%
problems with studying 18%
dystrophy 7% 28%
limbs pain 18%
congenital liver fibrosis 10% 29%
hepatosplenomegaly 18%
delayed motor development 23% 40%
enlargement of the liver and spleen 18%
night apnea 9% 26%
proteinuria 17%
permanent arrhythmia 8% 24%
forgetfulness 17%
hypotension with weakness 9% 25%
liquid stool 17%
hypotension 8% 23%
child is not says 17%
underdevelopment 7% 21%
hypertrophy biliary tract 17%
family man 7% 21%
ones weakness in the leg muscles 17%
weak ligaments 14% 28%
paresis 17%
weakness of the ligaments 13% 27%
chronic kidney failure 17%
muscle weakness 25% 39%
convulsive syndrome in children 17%
mental retardation 12% 25%
bipolar disorder 16%
ataxia 26% 39%
there are no complaints 16%
mental retardation 19% 32%
psychosis 16%
lags behind in the development 21% 34%
anamnesis ischemic stroke 16%
cerebellar ataxia 24% 36%
diseases of the gastrointestinal tract 16%
hypotension 9% 20%
kidney failure 16%
sensorineural 15% 26%
weakness in the legs 16%
impaired coordination 25% 36%
diseases of infants 16%
weakness 24% 35%
cataract 16%
hearing impaired 21% 31%
quickly gets tired 16%
nephropathy 15% 21%
enlarged liver 16%
cognitive disorders 17% 22%
end-stage renal failure 16%
congestive kidney 25% 30%
ophthalmoplegia 16%
arrhythmia 16% 21%
sharp change of mood 16%
chronic kidney disease 23% 28%
abdominal pain 16%
liver diseases 15% 19%
There is a noise 16%
kidney disease 15% 19%
stroke 16%
cardiac disorder 14% 18%
mental retardation 16%
speech slurred 20% 21%
tinnitus 15%
mood disorder 15%
cerebellar dysarthria 15%
abdominal pain after diarrhea 15%
pain in the wrists 15%
undisciplined 15%
blindness 15%
up mania 15%
confusion 15%
violation of the chair 15%
infantile 15%
demyelinating diseases 15%
worse when walking 15%
s eyes cloudy 15%
diarrhea 15%
madness 15%
depression 14%
high temperature 14%
pseudobulbar syndrome 14%
heart failure 14%
sad 14%
abdominal pain in the morning stomach 14%
angiopathy 14%
sadness 14%
delayed reaction 14%
a difficult teenager 14%
organic brain damage 14%
acute pain 14%
nose nursing mom 14%
common rashes 14%
stool with gases 14%
protein c deficiency 14%
median nerve neuropathy 14%
cerebral circulation disorder 14%
protein with increased 14%
transplant rejection reaction 14%
up imbecility 14%
up circulatory disorders 14%
epilepsy in the morning 14%
hematoma 13%
consequences of stroke 13%
sensations in the legs 13%
takes care of relatives 13%
constant pain 13%
twitching of the upper eyelid 13%
slowness of movement (bradykinesia) 13%
transient ischemic attack 13%
twitches eyelid 13%
portal hypertension 13%
lymphostasis 13%
skin problems 13%
diarrhea with gases 13%
ringing in the head 13%
the feeling of falling 13%
liver failure 13%
worse after midnight 13%
scarring 13%
heart dysfunction 13%

Instructions

Video
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  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 .
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