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Comparison results

 
Results: Differences General ✘Myotonic syndrome in children✘Lawrence-Moon-Bardet-Bidl syndrome
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Distinctive symptoms
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myotonia 69% —
retinitis pigmentosa — 89%
dystrophic myotonia 49% —
lawrence-moon-bardet-bidl syndrome — 85%
neuromyotonia 48% —
retinitis — 78%
myopathy 44% —
lawrence-moon-beadle syndrome — 77%
paroxysmal myoplegia 43% —
polydactyly — 76%
logorrhea 40% —
myopic chorioretinitis — 73%
oppenheim syndrome 39% —
congenital anomalies of the upper extremities — 72%
congenital myopathies 39% —
syndactyly — 68%
steinert 's disease 39% —
congenital anomalies of the lower extremities — 62%
ganglioneuritis 39% —
agenesis of the corpus callosum — 61%
sluggish baby 38% —
hypogonadism — 60%
muscle weakness 38% —
congenital myopia — 59%
relaxation 37% —
senile hyperopia — 55%
weakness in the legs 36% —
fundus arteries narrowed — 53%
birth trauma of the head 36% —
up vascular mesh — 51%
muscle tension 35% —
vitamin c increased — 51%
can not hold his head 35% —
not mindfulness — 50%
perinatal encephalopathy 35% —
obesity — 50%
head injury 34% —
limited vocabulary — 50%
paretic gait 34% —
teacher — 49%
damage to the nervous system 34% —
progressive myopia — 49%
inflammatory myopathy 34% —
hyperopia — 48%
paralysis 33% —
astigmatism — 48%
asymmetry 33% —
brachydactyly — 48%
paresis 32% —
patient is motionless — 48%
stiffness in the joints 32% —
deformity of the toes — 48%
sad 32% —
diabetes mellitus — 47%
hypoparathyroidism 32% —
deformity of the fingers — 47%
flaccid paralysis syndrome 32% —
obesity on the stomach — 46%
periodic paralysis 31% —
abdominal obesity — 46%
fatigue from children 30% —
dystrophy 31% 76%
paralysis of the lower extremities 30% —
anomalies of kidney development — 44%
paralysis of the limbs 30% —
fat deposits — 43%
postencephalitic syndrome 30% —
myopia — 42%
stiffness of movements 30% —
strabismus — 42%
leg weakness walking 30% —
deformity of fingers — 42%
weakness no 30% —
skeletal deformity — 42%
delayed motor development 29% —
deformity of the foot — 41%
cannot relax 29% —
shortening of legs — 41%
hormonal disorders 29% —
speech absence — 40%
rickets 28% —
angiopathy of the retina — 40%
weakness in the leg muscles 28% —
cataract — 40%
increased potassium 28% —
hyperlipidemia — 39%
paresis of legs 28% —
cholesterolemia — 39%
weakness in the hands 28% —
decreased intelligence — 39%
myxedema 27% —
curvature of the legs — 38%
neuroinfections 27% —
s eyes cloudy — 38%
delayed reaction 27% —
will not work — 37%
delay in physical development 27% —
weight change — 37%
trauma 27% —
ataxia — 37%
cns tumors 27% —
speech slurred — 36%
muscle atrophy 26% —
bone deformation — 36%
weakness in the extremities 26% —
arterial occlusion — 35%
encephalopathy 25% —
overweight — 35%
myotonia is congenital 25% —
impaired coordination — 35%
nervous excitability 25% —
decreased concentration of attention — 35%
delay of mental development 25% —
visual impairment — 34%
traumatic brain injury 25% —
convulsions — 33%
head tumor 25% —
control issues — 32%
increased motor activity 24% —
angiopathy — 31%
motor activity 24% —
inflammation 18% 48%
no children 24% —
there are no complaints — 30%
brain tumor 23% —
mental retardation 24% 53%
high height 23% —
delayed speech development 24% 53%
overexcitation of the psyche 23% —
children's speech 24% 52%
organic brain damage 22% —
increased 18% 38%
weakness after illness 21% —
neurological disorders 29% 45%
joint diseases 21% —
lowered 25% 39%
quickly gets tired 21% —
lags behind in the development 43% 57%
periodic illness 20% —
recovery period 20% 31%
swelling 20% —
stage of recovery 20% 31%
drug disease 19% —
oncology 18% 28%
rossolimo-steinert-kurschmann dystrophic myotonia 17% —
metabolic disorder 37% 46%
childhood diseases 43% 30%
helps others 30% 33%

Instructions

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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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