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Comparison results

 
Results: Differences General ✘Aicardi syndrome✘Nijmegen syndrome
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 24%(1)86%(4)
General blood test —97%(4)
MRI of the organ 39%(0)36%(0)
Coagulogram —71%(1)
CT of the organ 37%(0)34%(0)
Ultrasound of the organ 31%(0)34%(0)
Coprogram 26%(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%
aicardi syndrome 98% —
absolute lymphopenia — 97%
infantile 62% —
mastoiditis in children — 95%
epilepsy attacks 62% —
immunodeficiency — 88%
epilepsy 59% —
lymphopenia — 86%
asymmetry 59% —
frequent genyantritis — 81%
spasm 55% —
sinusitis in children — 81%
convulsions 54% —
arachnoid cyst of the brain — 75%
hemangiomas on the skin 54% —
Mongoloid — 73%
angiosarcoma 54% —
sinusitis in children — 70%
warts 51% —
mastoiditis — 67%
facial crevices 49% —
purulent genyantritis — 67%
dandy-walker syndrome 49% —
otitis media in children — 67%
impaired function of the cerebral hemispheres 49% —
hip dysplasia — 63%
diarrhea from dairy 47% —
polydactyly — 63%
hepatoblastoma 46% —
kidney dystopia — 63%
hemangioma 45% —
hypospadias — 62%
scoliosis 44% —
clinodactyly — 62%
hydrocephalus 43% —
frequent otitis — 61%
ventriculomegaly 42% —
viral otitis media — 61%
neonatal convulsions 41% —
reason for the consequences of puberty — 61%
spondylopathy 41% —
fracture of the humerus — 61%
curvature of the spine 40% —
genyantritis — 60%
crumpy syndrome 40% —
high height — 60%
microphthalmos 40% —
kidney aplasia — 60%
delay of mental development 40% —
milk rashes — 60%
delayed speech development 39% —
dyspepsia in children — 60%
mental retardation 39% —
acute otitis — 59%
myoclonic epilepsy 39% —
vitiligo, says a lot — 59%
retinitis pigmentosa 38% —
arvi in children — 58%
children's speech 38% —
periods of exacerbation — 57%
up imbecility 38% —
childhood diseases 22% 78%
nocturnal epilepsy attacks 38% —
chronic otitis — 56%
skin problems 37% —
shoulder injury — 56%
there are no characteristic signs 37% —
bronchitis in children — 56%
micrognathia 37% —
deformation of the skull — 55%
congenital anomalies of the upper extremities 37% —
cryptorchidism — 55%
seminoma 37% —
purulent otitis — 55%
2 children 37% —
purulent bronchitis — 55%
epilepsy at night 36% —
otitis media — 55%
tetraparesis 36% —
areas of depigmentation of the skin — 54%
spinal abnormalities 35% —
a difficult teenager — 54%
weak ligaments 35% —
acute otitis — 54%
facial spasms 35% —
a difficult life — 53%
different eyes 35% —
epstein barr virus — 53%
sharpness decreased vision 34% —
pneumonia in children — 53%
clonic cramps 34% —
immunoglobulin a deficiency — 51%
intestinal polyp 34% —
false joint — 51%
weakness in the arms and legs 34% —
otitis — 50%
big ears 34% —
periodic illness — 50%
weakness of the muscles of the hands 34% —
primary immunodeficiency — 49%
tonic convulsions 34% —
lower respiratory tract infections — 49%
premature sexual development 34% —
worse at 11 o'clock — 49%
eye development abnormalities 34% —
solid tumors — 49%
cramps at night 34% —
viral pneumonia — 49%
epilepsy in children 33% —
sinusitis — 49%
weakness of the ligaments 33% —
delay in physical development — 48%
retinal dystrophy 33% —
rash on the body — 48%
retinitis 33% —
big head — 48%
lot of moles 33% —
history medical mother's — 47%
paresis of the hand 33% —
patient's condition — 47%
that's diarrhea constipation 33% —
common rashes — 47%
delayed puberty 33% —
smart baby — 46%
paresis of legs 32% —
Chronical bronchitis — 46%
congenital anomalies of the lower extremities 32% —
j42 chronic bronchitis — 46%
digestion constipation 32% —
omission of internal organs — 46%
grumpy 32% —
bacterial pneumonia — 46%
facial asymmetry 32% —
difficult childhood — 46%
weakness in the leg muscles 32% —
acute bronchitis — 46%
twitching of the upper eyelid 32% —
cytomegalovirus — 45%
twitches eyelid 32% —
microcephaly 36% 81%
weakness in the hands 32% —
weakening of immunity — 44%
convulsive syndrome in children 32% —
effects of puberty — 44%
optic nerve atrophy 32% —
ARVI — 44%
in the genus mental illness 31% —
bronchitis — 44%
double vision 31% —
lowered 29% 72%
reflux esophagitis 31% —
fistula — 43%
hypotension with weakness 31% —
herpes — 43%
tics 30% —
short height — 42%
bowel cancer 30% —
skin spots — 42%
high intelligence 30% —
frequent colds — 42%
weakness in the extremities 30% —
digestive disorders — 41%
polyps 29% —
a history of organ transplantation — 41%
history of brain surgery 29% —
pneumonia — 40%
cataract 29% —
bone fracture — 40%
skin cancer 29% —
radiation damage — 39%
weakness in the legs 29% —
changes in the blood — 39%
decreased intelligence 29% —
control issues — 38%
s eyes cloudy 28% —
impaired kidney function — 38%
large child 28% —
impaired lung function — 36%
intestinal tumor 28% —
diseases of the gastrointestinal tract — 35%
nervousness 27% —
consequences of infection — 35%
blurred vision 27% —
trauma — 34%
unformed feces 26% —
orbital hypertelorism 34% 55%
constipation 26% —
syndactyly 35% 56%
paresis 26% —
brain cyst 37% 58%
bone deformation 26% —
harelip 32% 52%
nose nursing mom 26% —
big nose 35% 55%
early development 26% —
skeletal deformity 31% 49%
vascular tumor 25% —
bone defects 28% 44%
dystrophy 25% —
cancer 23% 37%

Instructions

Video
  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.
  4. The list changes dynamically depending on the data of the current visit in the selection of therapy .
  5. Click on the percentageto see the suggestions from the original source.
  6. By using the service, you agree to user agreement.
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