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Comparison results

 
Results: Differences General ✘Sluggish child syndrome✘Joubert syndrome
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 84%(5)—
Elements and vitamins 43%(1)—
MRI of the organ —37%(0)
CT of the organ —35%(0)
Ophthalmologist's examination —22%(0)
MRI of the brain —21%(0)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 100%—
Register, to see more distinctive signs of diseases and studies —100%
hysterical 95% —
encephalocele — 57%
oppenheim syndrome 94% —
polycystic liver — 52%
ganglioneuritis 94% —
coloboma — 47%
congenital myopathies 94% —
liver cyst — 43%
increased ldh 84% —
rapid breathing — 42%
inflammatory myopathy 83% —
ataxia — 40%
hoffmann 's perifolliculitis 64% —
retinal dystrophy — 39%
myopathy 63% —
polycystic liver disease — 39%
werdnig-hoffman amyotrophy 58% —
delayed motor development — 39%
galactosemia 58% —
kidney cyst — 38%
spinal amyotrophy 58% —
cerebellar ataxia — 37%
flaccid paralysis syndrome 49% —
impaired coordination — 37%
cerebral palsy 43% —
polycystic — 36%
weakness is worse from movement 40% —
apnea — 35%
muscle atrophy 40% —
hydrocephalus — 35%
facial muscle weakness 39% —
cystic fibrosis — 34%
phenylketonuria 38% —
idiocy — 33%
paralysis 36% —
cirrhosis of the liver — 33%
rapid reaction 36% —
akathisia — 33%
weakness in the hip 36% —
hearing impaired — 32%
worse from movement 35% —
brain development abnormalities — 32%
myasthenia 35% —
bradypnea — 31%
weakness in the foot 35% —
up vascular mesh — 31%
spinal cord injury 34% —
congestive kidney — 31%
glycogenoses 34% —
ataxia in children — 31%
strongest weakness 34% —
better from movement — 30%
marfan syndrome 34% —
congenital liver fibrosis — 30%
down syndrome 33% —
polycystic kidney — 30%
impaired function of the cerebral hemispheres 33% —
neuritis of the auditory nerve — 29%
metabolic disorder 33% —
cysts — 29%
weakness no 33% —
dystrophy — 29%
increase in creatine kinase 32% —
weak ligaments — 29%
mitochondrial myopathy 32% —
involuntary movements — 28%
rickets 31% —
hearing loss in children — 28%
weakness in the leg muscles 31% —
change of teeth — 28%
muscular dystrophy 31% —
weakness of the eyes — 27%
hyperkinesis 30% —
night apnea — 27%
weak joints 30% —
weakness of the ligaments — 27%
damage to the nervous system 30% —
respiratory arrest in a dream — 27%
spinal injury 29% —
sensorineural — 27%
weakness in the legs 28% —
breath retention — 27%
inflammation of the brain 27% —
anomalies of kidney development — 27%
muscle hypertonus 27% —
weak breathing — 27%
childhood diseases 47% 18%
nystagmus — 26%
calculating 25% —
weakness when breathing — 25%
inflammation 44% 17%
deafness — 25%
traumatic illness 25% —
weakness during the day — 25%
hypotension 47% 20%
big head — 25%
spasm 24% —
growth disorders in children — 24%
patient is motionless 24% —
permanent arrhythmia — 24%
trauma 21% —
neuritis — 24%
impaired arterial function 21% —
inflammation of the eyes — 24%
increased 19% —
history of brain surgery — 24%
nemaline myopathy 19% —
eye surgery — 23%
sluggish baby 50% 35%
neuralgia — 23%
hypotension with weakness 30% 26%
constantly moving — 22%
cognitive disorders 26% 22%
speech slurred — 22%
hypotension 27% 23%
nephropathy — 22%
intellectual disabilities in children 29% 25%
family man — 21%
arrhythmia — 21%
impaired kidney function — 20%
liver problems — 20%
neurological disorders — 19%
impaired venous function — 19%
angioplasty — 18%
history of surgery — 17%
weakness after illness 23% 34%
lags behind in the development 33% 40%
smart baby 28% 34%
lowered 19% 24%
mental retardation 27% 32%
muscle weakness 41% 41%

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.
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