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Comparison results

 
Results: Differences General ✘Mitochondrial diseases✘Morchio 's disease
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 100%(2)100%(2)
General urine test 42%(10)88%(1)
General blood test 44%(9)65%(2)
ECG 42%(0)65%(0)
Ultrasound of abdominal cavity 38%(0)57%(0)
Radiography of the cervical spine —80%(0)
Ultrasound of the Heart 37%(0)38%(0)
Spirometry —64%(0)
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 25%—
Register, to see more distinctive signs of diseases and studies —65%
chilly 21% —
morchio 's disease — 43%
encephalopathy 20% —
chest deformity — 39%
melas syndrome 18% —
curvature of the spine — 39%
weak heart 18% —
deformities of the limbs — 38%
ray 's syndrome 17% —
joint deformation — 38%
beriberi 17% —
hump — 37%
vitamin b2 lowered 16% —
lumbar kyphosis — 36%
liver failure 16% —
corneal opacity — 36%
leber's hereditary optical neuropathy 15% —
hepatosplenomegaly — 33%
citrullinemia 15% —
compression of the spinal cord — 33%
myoglobinuria 15% —
kyphosis scoliosis — 33%
lethargy 15% —
scoliosis — 33%
hellp syndrome 15% —
joint diseases — 33%
disorders of consciousness 15% —
contractures of the joints — 32%
quickly gets tired 14% —
enlargement of the spleen 5% 37%
fatigue feeling 14% —
valgus deformity of the foot — 32%
dilated cardiomyopathy 14% —
stiffness in the joints — 32%
muscle pain from exertion 13% —
spondylopathy — 31%
twitches eyelid 13% —
enlargement of the liver and spleen 5% 36%
twitching of the upper eyelid 13% —
neck is short — 31%
appetite immediately after eating 13% —
curvature of the legs 5% 35%
acute liver failure 13% —
skeletal deformity — 30%
sudden infant death syndrome 13% —
trunk is shortened — 30%
redness of the upper eyelid 13% —
bone deformation — 30%
hypertrophic cardiomyopathy 13% —
calve's disease — 29%
diabetic encephalopathy 13% —
sanfilippo syndrome — 28%
diabetic cardiomyopathy 13% —
hydrocephalus — 28%
pearson 's syndrome 13% —
frequent otitis — 28%
fasting 13% —
coarsening of facial features — 28%
rhabdomyolysis 13% —
muscle tension — 27%
hepatoses 12% —
thoracolumbar kyphosis — 27%
death of the child 12% —
osteochondropathy — 27%
pain intolerance 12% —
umbilical hernia — 27%
liver atrophy 12% —
hearing impaired 9% 35%
listlessness drowsiness 12% —
thoracic kyphosis — 26%
sepsis 12% —
hernia of the abdomen — 25%
sucks in the stomach 12% —
night apnea — 25%
necrosis 12% —
hernia — 25%
tics 12% —
otitis — 25%
hepatosis fatty 12% —
respiratory arrest in a dream — 25%
tonic-clonic convulsions 12% —
enlarged liver 10% 35%
oncology 11% —
x-shaped legs — 25%
increase in creatine kinase 11% —
deformity of the foot 5% 29%
clonic cramps 11% —
alpha-mannosidosis — 24%
muscle fatigue 11% —
contracture 5% 29%
vomiting food 11% —
clumsiness — 23%
vomiting during meals 11% —
history of surgery 7% 30%
barth syndrome 11% —
dwarfism — 22%
generalized epilepsy 11% —
arthritis — 22%
sluggish baby 11% —
adenoids — 22%
not enough freedom 11% —
curvature of the shins — 22%
reduced energy 11% —
stunting — 21%
hypoglycemia 11% —
skin compaction — 21%
metabolic acidosis 11% —
epiphyseal dysplasia — 21%
zinc 11% —
constantly swallows saliva — 21%
weakness in the heart 11% —
inguinal hernia — 20%
hyperinsulinism 11% —
epiglottis hypertrophy — 20%
food is poorly digested 11% —
spinal epidural abscess — 20%
vomiting bile 11% —
aspiration pneumonia — 20%
optic nerve atrophy 11% —
chronic otitis — 20%
coma 11% —
tension in the face — 20%
vomiting bile in the morning 10% —
laryngeal tonsils — 20%
feeling of a coma in the stomach 10% —
pneumonia vomiting — 20%
hypoglycemic coma 10% —
chronic respiratory failure 5% 25%
history medical mother's 10% —
tonsils thickening — 19%
eats often 10% —
paresis — 19%
feeling of bruising 10% —
No saliva — 19%
urine light 10% —
underdevelopment — 19%
vomiting blood 10% —
myelopathy — 19%
drowsiness during the day 10% —
lowered 13% 32%
the child does not eat 10% —
wide shoulders — 19%
coma in a child 10% —
weakness of the bladder — 19%
diarrhea with undigested food 10% —
childhood diseases 13% 32%
brown urine 10% —
dislocation of the forearm — 18%
muscle pain 10% —
false joint — 18%
intoxication with iron preparations 10% —
tendon compaction — 18%
diabetes mellitus 10% —
her hair is hard — 18%
weakness after eating 10% —
restless hands — 18%
diarrhea after eating 10% —
polyarthritis — 18%
diseases of infants 10% —
gastroneurosis — 18%
epilepsy in children 10% —
elbow joint contracture — 18%
parkinson's disease 10% —
knee joint contracture — 18%
vertical size of liver is increased 10% —
kyphosis cervicothoracic — 18%
kidney failure 10% —
respiratory insufficiency 8% 26%
pain from the load 10% —
heart failure 15% 32%
absences 10% —
megalocornea — 17%
zpr fatigue from the disease 10% —
inflammation 12% 29%
overwork 10% —
hypertrophy of the tonsils — 17%
ley syndrome 10% —
difficult to swallow — 17%
pain during exercise 10% —
joints unstable — 17%
polyneuropathy 10% —
pneumonia with bronchitis — 17%
arrhythmia weakness 10% —
contracture of the hands — 17%
chronic liver failure 10% —
pneumonia — 17%
myopathy 22% 10%
otitis media due to a runny nose — 17%
glutaric aciduria 10% —
there is heart failure 15% 32%
pancytopenia 9% —
spinal canal stenosis — 17%
responsible 9% —
stooped — 17%
weakness after diarrhea 9% —
cervical kyphosis — 17%
attacks of pain 9% —
frequent swallowing — 17%
blindness 9% —
hearing loss in children — 16%

Instructions

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  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.
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