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Comparison results

 
Results: Differences General ✘Crouzon syndrome✘Ahlstrom syndrome
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Distinctive symptoms
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synostosis 85% —
kalman syndrome — 86%
divergent squint 72% —
hypogonadism — 82%
exophthalmos 63% —
photophobia — 79%
atresia hoan 63% —
dilated cardiomyopathy — 78%
craniosynostosis 57% —
testicular atrophy — 77%
aper syndrome 54% —
ahlstrom syndrome — 77%
brachycephaly 53% —
metabolic syndrome — 76%
strabismus 51% —
thyroid atrophy — 74%
pfeiffer syndrome 51% —
pancreatic atrophy — 74%
atresia of the auditory canal 51% —
hormonal disorders — 72%
blepharophimosis 48% —
increased uric acid — 71%
rubs the nose 46% —
sensorineural — 70%
occlusive hydrocephalus 45% —
cardiodilation — 70%
lot of moles 44% —
up vascular mesh — 70%
black moles 43% —
insulin increase — 69%
history of surgery 42% —
obesity — 69%
bone growths 42% —
type 2 diabetes mellitus — 67%
hyperkeratosis 41% —
uric acid of urine is elevated — 65%
lags behind in the development 40% —
hereditary hearing loss — 64%
moles on the face 38% —
diabetes mellitus — 64%
keratinized warts 37% —
ovarian hypoplasia — 63%
hearing loss 36% —
cardiomyopathy — 62%
childhood diseases 36% —
ovarian endometriosis — 62%
brown moles 35% —
contains several folds — 60%
multiple warts 34% —
testicular cyst — 60%
intrauterine fetal development delay 33% —
defects of dentition — 60%
orbital hypertelorism 33% —
proteinuria — 59%
big nose 33% —
blurred vision — 59%
syndactyly 33% —
heart dysfunction — 59%
convulsions pain 32% —
thyroid cyst — 58%
hearing loss in children 32% —
retinitis pigmentosa — 57%
vomiting 32% —
nephropathy — 57%
impaired venous function 32% —
glycohemoglobin increased — 57%
overflow of the head 31% —
uterine hypoplasia — 57%
there is no head 29% —
retinal atrophy — 56%
nose large eyes 29% —
blood diseases — 56%
hydrocephalus 29% —
congenital hypothyroidism — 55%
increased intracranial pressure 28% —
brachydactyly — 54%
dislocation 28% —
in the family diabetes — 54%
warts 28% —
uterine appendages are increase — 54%
age 4 years 28% —
polycystic ovaries — 53%
difficulty breathing 27% —
increased triglycerides — 53%
head surgery 27% —
uterine cyst — 53%
brain tumors 26% —
hirsutism — 53%
mental retardation 26% —
cryptorchidism — 52%
large child 26% —
impaired glucose tolerance — 52%
elderly patients 26% —
enlargement of the uterus — 52%
impaired nervous system function 26% —
endometriosis — 51%
short height 25% —
dystrophy 33% 84%
brain tumor 25% —
retinitis — 50%
convulsions 23% —
heart transplantation — 50%
surgical infections 22% —
ovarian cysts — 50%
neurological disorders 22% —
eats often — 50%
damage to the nervous system 21% —
hypertension — 50%
oncology 20% —
increased hairiness — 49%
papillomatous nevus 19% —
baldness — 49%
can't hold urine — 49%
amenorrhea — 48%
ovarian dysfunction — 48%
hepatosis fatty — 48%
hepatosis — 48%
heart disease in the genus — 47%
liver atrophy — 47%
urinary incontinence — 47%
insulin deficiency — 47%
hyperpigmentation — 47%
nystagmus — 47%
polycystic — 47%
skeletal deformity — 47%
deformity of fingers — 47%
hair loss — 46%
pancreatopathy — 46%
hemoglobin increased — 46%
hepatosplenomegaly — 46%
enlargement of the liver and spleen — 45%
type 1 diabetes mellitus — 45%
hyperlipidemia — 44%
increased appetite — 44%
decreased intelligence — 44%
chronic kidney disease — 44%
cholesterolemia — 44%
cystic fibrosis — 44%
enlargement of the spleen — 43%
hypoglycemia — 43%
curvature of the spine — 43%
hyperglycemia — 42%
impaired uterine function — 42%
consultation with a cardiologist — 42%
little urine — 42%
weight change — 42%
hypothyroidism — 42%
appendages of the uterus — 41%
enlargement of the heart — 41%
nervousness — 41%
oily skin — 41%
increased 27% 68%
protein c deficiency — 40%
enlarged liver — 40%
protein with increased — 40%
overweight — 39%
a history of organ transplantation — 39%
there is heart failure — 38%
heart failure — 38%
family man — 38%
cysts — 38%
angioplasty 21% 58%
impaired kidney function — 36%
hearing impaired 58% 92%
there are no complaints — 33%
inflammation — 31%
visual impairment 34% 54%
deafness 49% 64%
patient's condition 20% 31%
lowered 33% 43%
black acanthosis 65% 74%
the skin is dark 38% 43%
skin dystrophy 46% 51%

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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