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Comparison results

 
Results: Differences General ✘Primary systemic carnitine deficiency✘Myotonic syndrome in children
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 98%(2)—
Coagulogram 59%(1)—
Ultrasound of the organ 58%(0)—
MRI of the organ —39%(0)
CT of the organ —38%(0)
General urine test 38%(0)—
General blood test 35%(1)—
Thyroid hormones —28%(1)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 100%—
Register, to see more distinctive signs of diseases and studies —100%
hypoglycemia 98% —
myotonia — 69%
beriberi 93% —
dystrophic myotonia — 49%
citrullinemia 86% —
neuromyotonia — 48%
weak heart 83% —
myopathy — 44%
weakness in the heart 80% —
paroxysmal myoplegia — 43%
arvi in children 79% —
logorrhea — 40%
dilated cardiomyopathy 79% —
steinert 's disease — 39%
decrease in creatine kinase 78% —
congenital myopathies — 39%
heart dysfunction 77% —
ganglioneuritis — 39%
blood diseases 74% —
oppenheim syndrome — 39%
indifference to children 72% —
relaxation — 37%
primary systemic carnitine deficiency 68% —
birth trauma of the head — 36%
shortness of breath during physical exertion 68% —
weakness in the legs — 36%
dyspnea 66% —
perinatal encephalopathy — 35%
hypoglycemic coma 64% —
can not hold his head — 35%
pectoris cardiac dyspnea 64% —
muscle tension — 35%
vomiting 63% —
head injury — 34%
ARVI 61% —
inflammatory myopathy — 34%
fear of vomiting 61% —
paretic gait — 34%
cold weakness 60% —
paralysis — 33%
pain in the heart during exercise 60% —
asymmetry — 33%
enlargement of the heart 59% —
paresis — 32%
cardiodilation 58% —
stiffness in the joints — 32%
anxiety on the heart 58% —
sad — 32%
enlarged liver 57% —
hypoparathyroidism — 32%
there is heart failure 54% —
flaccid paralysis syndrome — 32%
heart failure 54% —
dystrophy — 31%
child's poor appetite 54% —
periodic paralysis — 31%
increase in creatine kinase 52% —
paralysis of the limbs — 30%
fasting 52% —
leg weakness walking — 30%
feeling of lack of air 50% —
paralysis of the lower extremities — 30%
appetite is poor 50% —
helps others — 30%
often sick child 50% —
postencephalitic syndrome — 30%
increased 69% 18%
fatigue from children — 30%
consequences of a viral infection 48% —
stiffness of movements — 30%
need for fats 48% —
cannot relax — 29%
angioplasty 48% —
hormonal disorders — 29%
compressing pains in the heart 47% —
delayed motor development — 29%
muscle fatigue 47% —
weakness in the leg muscles — 28%
little low energy level 47% —
weakness in the hands — 28%
apathy 46% —
increased potassium — 28%
vomiting multiple 46% —
paresis of legs — 28%
discharge phobias 46% —
rickets — 28%
fears of anxiety 46% —
trauma — 27%
coma 45% —
cns tumors — 27%
fear of illness 44% —
myxedema — 27%
memory impairment 44% —
neuroinfections — 27%
tumors of the heart 44% —
delayed reaction — 27%
little urine 43% —
muscle atrophy — 26%
pain during exercise 43% —
weakness in the extremities — 26%
liver failure 43% —
traumatic brain injury — 25%
lowered 70% 25%
nervous excitability — 25%
forced situation 43% —
delay of mental development — 25%
forgetfulness 42% —
head tumor — 25%
pain in the heart 42% —
myotonia is congenital — 25%
impaired nervous system function 41% —
encephalopathy — 25%
pain from the load 41% —
children's speech — 24%
frequent colds 41% —
delayed speech development — 24%
short height 41% —
no children — 24%
2 children 40% —
motor activity — 24%
weakness after illness 63% 21%
mental retardation — 24%
anxiety 39% —
increased motor activity — 24%
family man 39% —
overexcitation of the psyche — 23%
no appetite 39% —
brain tumor — 23%
pain chest 39% —
high height — 23%
psychologist 38% —
organic brain damage — 22%
immunodeficiency 38% —
joint diseases — 21%
hematuria 38% —
swelling — 20%
zpr fatigue from the disease 38% —
stage of recovery — 20%
presses 37% —
recovery period — 20%
stress 37% —
periodic illness — 20%
liver problems 36% —
rossolimo-steinert-kurschmann dystrophic myotonia — 17%
there are no complaints 34% —
consequences of infection 34% —
patient's condition 32% —
quickly gets tired 53% 21%
metabolic disorder 65% 37%
muscle weakness 66% 38%
childhood diseases 67% 43%
weakness no 52% 30%
delay in physical development 46% 27%
drug disease 34% 19%
oncology 32% 18%
inflammation 32% 18%
lags behind in the development 53% 43%
sluggish baby 47% 38%
neurological disorders 36% 29%

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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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