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Comparison results

 
Results: Differences General ✘Lawrence-Moon-Bardet-Bidl syndrome✘Ahlstrom syndrome
Related research Analogs Analogs
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 85%—
Register, to see more distinctive signs of diseases and studies —92%
lawrence-moon-beadle syndrome 77% —
kalman syndrome — 86%
polydactyly 76% —
photophobia — 79%
myopic chorioretinitis 73% —
dilated cardiomyopathy — 78%
congenital anomalies of the upper extremities 72% —
testicular atrophy — 77%
syndactyly 68% —
ahlstrom syndrome — 77%
congenital anomalies of the lower extremities 62% —
metabolic syndrome — 76%
agenesis of the corpus callosum 61% —
pancreatic atrophy — 74%
congenital myopia 59% —
black acanthosis — 74%
lags behind in the development 57% —
thyroid atrophy — 74%
senile hyperopia 55% —
hormonal disorders — 72%
delayed speech development 53% —
increased uric acid — 71%
mental retardation 53% —
cardiodilation — 70%
fundus arteries narrowed 53% —
sensorineural — 70%
children's speech 52% —
insulin increase — 69%
vitamin c increased 51% —
type 2 diabetes mellitus — 67%
not mindfulness 50% —
uric acid of urine is elevated — 65%
limited vocabulary 50% —
hereditary hearing loss — 64%
progressive myopia 49% —
deafness — 64%
teacher 49% —
ovarian hypoplasia — 63%
astigmatism 48% —
ovarian endometriosis — 62%
deformity of the toes 48% —
cardiomyopathy — 62%
patient is motionless 48% —
testicular cyst — 60%
hyperopia 48% —
contains several folds — 60%
deformity of the fingers 47% —
defects of dentition — 60%
metabolic disorder 46% —
proteinuria — 59%
abdominal obesity 46% —
heart dysfunction — 59%
obesity on the stomach 46% —
blurred vision — 59%
neurological disorders 45% —
thyroid cyst — 58%
anomalies of kidney development 44% —
angioplasty — 58%
fat deposits 43% —
uterine hypoplasia — 57%
strabismus 42% —
nephropathy — 57%
myopia 42% —
glycohemoglobin increased — 57%
shortening of legs 41% —
retinal atrophy — 56%
deformity of the foot 41% —
blood diseases — 56%
speech absence 40% —
congenital hypothyroidism — 55%
angiopathy of the retina 40% —
in the family diabetes — 54%
cataract 40% —
uterine appendages are increase — 54%
s eyes cloudy 38% —
polycystic ovaries — 53%
curvature of the legs 38% —
increased triglycerides — 53%
ataxia 37% —
uterine cyst — 53%
will not work 37% —
hirsutism — 53%
bone deformation 36% —
cryptorchidism — 52%
speech slurred 36% —
impaired glucose tolerance — 52%
arterial occlusion 35% —
enlargement of the uterus — 52%
impaired coordination 35% —
skin dystrophy — 51%
decreased concentration of attention 35% —
endometriosis — 51%
convulsions 33% —
ovarian cysts — 50%
helps others 33% —
eats often — 50%
control issues 32% —
heart transplantation — 50%
recovery period 31% —
hypertension — 50%
stage of recovery 31% —
baldness — 49%
angiopathy 31% —
increased hairiness — 49%
childhood diseases 30% —
can't hold urine — 49%
retinitis pigmentosa 89% 57%
hepatosis fatty — 48%
oncology 28% —
amenorrhea — 48%
retinitis 78% 50%
ovarian dysfunction — 48%
inflammation 48% 31%
hepatosis — 48%
polycystic — 47%
hyperpigmentation — 47%
insulin deficiency — 47%
heart disease in the genus — 47%
liver atrophy — 47%
urinary incontinence — 47%
nystagmus — 47%
pancreatopathy — 46%
hair loss — 46%
hepatosplenomegaly — 46%
hemoglobin increased — 46%
enlargement of the liver and spleen — 45%
type 1 diabetes mellitus — 45%
increased appetite — 44%
chronic kidney disease — 44%
cystic fibrosis — 44%
the skin is dark — 43%
curvature of the spine — 43%
enlargement of the spleen — 43%
hypoglycemia — 43%
hypothyroidism — 42%
hyperglycemia — 42%
impaired uterine function — 42%
consultation with a cardiologist — 42%
little urine — 42%
enlargement of the heart — 41%
appendages of the uterus — 41%
nervousness — 41%
oily skin — 41%
enlarged liver — 40%
protein c deficiency — 40%
protein with increased — 40%
a history of organ transplantation — 39%
family man — 38%
cysts — 38%
heart failure — 38%
there is heart failure — 38%
impaired kidney function — 36%
patient's condition — 31%
increased 38% 68%
hypogonadism 60% 82%
visual impairment 34% 54%
obesity 50% 69%
up vascular mesh 51% 70%
diabetes mellitus 47% 64%
dystrophy 76% 84%
brachydactyly 48% 54%
weight change 37% 42%
cholesterolemia 39% 44%
hyperlipidemia 39% 44%
decreased intelligence 39% 44%
deformity of fingers 42% 47%
skeletal deformity 42% 47%
overweight 35% 39%
lowered 39% 43%
there are no complaints 30% 33%
retinal dystrophy 100% 100%

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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.
  4. The list changes dynamically depending on the data of the current visit in the selection of therapy .
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