⬆
X
By continuing to use the site, you allow the use of Cookies and agree to the privacy policy.
.,о.,р..и.:г,.и.,н.;н.,а;,л.. .,н.:а,.х.,о.,д.;и.,т..с.:я,, ..н.;а., .,k;,i..b.:e,;r.,i.,s.,.;.r.:u,

Comparison results

 
Results: Differences General ✘Congenital hyperplasia of the adrenal cortex✘Canavan's disease
Related research Analogs Analogs
Distinctive symptoms
Register, to see more distinctive signs of diseases and studies 29%—
Register, to see more distinctive signs of diseases and studies —35%
congenital adrenal hyperplasia 28% —
metabolic disorder — 28%
adrenal hyperplasia 23% —
epilepsy attacks — 27%
excess acth 17% —
hepatosplenomegaly — 27%
adrenogenital syndrome 17% —
enlargement of the liver and spleen — 27%
aper syndrome 17% —
increased 6% 32%
male pseudohermaphroditism 16% —
enlargement of the spleen — 26%
female pseudohermaphroditism 16% —
difficult to swallow — 26%
excess aldosterone 13% —
niemann-pick disease — 26%
female hypospadias 13% —
epilepsy — 26%
acth deficiency 12% —
childhood diseases 11% 36%
hyperandrogenism in women 12% —
onset of illness — 25%
adrenal insufficiency in children 12% —
gaucher's disease — 24%
hypospadias 11% —
enlarged liver — 24%
gynecomastia 11% —
convulsions — 24%
arterial hypertension in children 10% —
porous skin — 23%
ovarian insufficiency 10% —
wolman 's disease — 23%
ovarian hypofunction 10% —
rashes dry — 23%
decreased potassium 9% —
history of surgery 8% 31%
worse at 11 o'clock 9% —
lowered 8% 30%
miscarriage 9% —
lags behind in the development — 22%
high height 8% —
fabry's disease — 22%
c21 6% —
angioceratoma — 22%
cortisol deficiency 16% 9%
volume of spleen is increased — 22%
delayed puberty 14% 8%
narcolepsy — 22%
drug disease — 22%
patient's condition — 22%
increased LDL — 21%
consequences of taking medications — 21%
liver problems — 21%
the onset of the disease during puberty — 21%
portal hypertension — 21%
hypersplenism — 21%
increased HDL — 20%
роды и вскармливание — 20%
alt reduction — 20%
neurological disorders — 20%
muscle weakness — 20%
reduction of HDL — 20%
lipoidosis — 20%
heart dysfunction — 20%
reduction of LDL — 19%
impaired arterial function — 19%
diseases of the gastrointestinal tract — 19%
slowness of movement — 19%
reduction of ast — 19%
increased cholesterol levels in the blood — 19%
a history of organ transplantation — 19%
macrocephaly — 19%
liver transplantation — 19%
blood diseases — 19%
congenital liver fibrosis — 19%
familial endogenous hypertriglyceridemia — 19%
cholestasis — 19%
impaired venous function — 18%
history of liver surgery — 18%
diarrhea — 18%
progressive supranuclear paralysis — 18%
splenectomy — 18%
lower cholesterol — 18%
impaired spleen function — 18%
there is heart failure — 18%
heart failure — 18%
thrombocytopenia — 18%
enteropathy — 18%
increased ast — 18%
gastrointestinal problems — 18%
damage to the nervous system — 18%
unformed feces — 18%
hearing impaired — 18%
dry — 18%
hypotension with weakness — 18%
malabsorption — 18%
liver failure — 18%
primary hypercholesterolemia — 18%
cholesterolemia — 17%
cardiac cirrhosis of the liver — 17%
control issues — 17%
hypertrophy of the left ventricle — 17%
congenital anomalies of the lower extremities — 17%
hepatosis fatty — 17%
hyperlipidemia — 17%
liver dysfunction — 17%
hemorrhagic diathesis — 17%
rupture duodenal dysfunction — 17%
hepatosis — 17%
sluggish baby — 17%
high temperature — 17%
expansion of the esophagus — 17%
adynamia — 17%
paranoia — 17%
cognitive disorders — 17%
intestinal insufficiency syndrome — 17%
leukopenia — 17%
there are no complaints — 17%
increased alt — 17%
swelling of the legs — 16%
affective disorders — 16%
infantile — 16%
angiopathy — 16%
periodic illness — 16%
corneal opacity — 16%
chronic heart failure — 16%
muscular dystonia — 16%
violation of the stool — 16%
polyneuropathy — 16%
hypertrophy biliary tract — 16%
ataxia — 16%
impaired lung function — 16%
arrhythmia — 16%
suspicion — 16%
calcification — 16%
hypotension — 16%
CHD — 16%
chronic venous edema — 16%
abdominal pain — 16%
need for fats — 16%
effects of puberty — 16%
epilepsy in the morning — 16%
early development — 16%
liver atrophy — 16%
stroke — 16%
dyslipidemia — 16%
kidney transplantation — 16%
quickly gets tired — 16%
anemia — 16%
hypotension — 16%
cirrhosis of the liver — 16%
ascites — 16%
general swelling does — 16%
steatorrhea — 15%
increased bleeding — 15%
abdominal pain after diarrhea — 15%
chronic kidney failure — 15%
angioplasty — 15%
impaired kidney function — 15%
pathological fracture — 15%
venous congestion — 15%
nose nursing mom — 15%
neurological pain — 15%
madness — 15%
anomalies of esophageal development — 15%
memory impairment — 15%
2 children — 15%
confusion of consciousness — 15%
up circulatory disorders — 15%
necrosis — 15%
swelling — 15%
impaired coordination — 15%
delirium — 15%
limbs pain — 15%
abdominal swelling — 15%
joint diseases — 15%
heart hypertrophy — 15%
hemophagocytic syndrome — 15%
neurogenic pain — 15%
end-stage renal failure — 14%
ophthalmoplegia — 14%
a difficult teenager — 14%
clonic cramps — 14%
cytolysis syndrome — 14%
bipolar disorder — 14%
generalized epilepsy — 14%
vomiting — 14%
abundant stool — 14%
cataract — 14%
fever intermittent — 14%
optimistic — 14%
I can't be alone — 14%
cerebral circulation disorder — 14%
tonic-clonic convulsions — 14%
kidney failure — 14%
median nerve neuropathy — 14%
bloating — 14%
proteinuria — 14%
forgetfulness — 14%
converging strabismus — 14%

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.