Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 36% —
Register , to see more distinctive signs of diseases and studies — 35%
lipoid nephrosis
33%
—
metabolic disorder —
27%
nephrotic syndrome
41%
9%
niemann-pick disease —
26%
nephrosis
29%
—
brain damage —
25%
hypoproteinemia
28%
—
epilepsy attacks —
24%
hematuria
25%
—
wolman 's disease —
24%
berger 's disease
24%
—
epilepsy —
23%
changes in urine
22%
—
fabry's disease —
23%
inflammation of the kidneys
30%
7%
porous skin —
23%
little urine
21%
—
another refined dermatitis —
23%
acute glomerulonephritis
21%
—
angioceratoma —
23%
facial swelling
20%
—
rashes dry —
23%
hereditary jade
20%
—
enlargement of the spleen —
22%
alport syndrome
20%
—
difficult to swallow —
22%
chilly with thirst
19%
—
hypersplenism —
22%
hematuric nephritis
19%
—
narcolepsy —
22%
crystalluria
18%
—
hepatosplenomegaly —
22%
microhematuria
18%
—
enlargement of the liver and spleen —
22%
nephrosclerosis
18%
—
convulsions —
21%
oliguria
17%
—
the onset of the disease during puberty —
21%
malaria
17%
—
increased LDL —
21%
leukocyturia
17%
—
onset of illness —
21%
kidney failure in children
17%
—
alt reduction —
20%
swelling of eyelids
16%
—
lags behind in the development —
20%
anasarka
16%
—
reduction of ast —
20%
antinuclear factor
16%
—
reduction of HDL —
20%
proteinuria
33%
15%
pregnancy —
20%
rapidly progressive glomerulonephritis
15%
—
increased HDL —
20%
mercury poisoning
15%
—
portal hypertension —
20%
antineutrophilic cytoplasmic antibodies
15%
—
familial endogenous hypertriglyceridemia —
19%
intestinal lymphoma
15%
—
reduction of LDL —
19%
pale puffy face
15%
—
primary hypercholesterolemia —
19%
oily facial skin
15%
—
cholestasis —
19%
remission
15%
—
liver failure —
19%
antithrombin is elevated
14%
—
slowness of movement —
19%
uremia
14%
—
liver transplantation —
19%
glomerulonephritis in children
14%
—
pure hypercholesterolemia —
19%
violation of protein metabolism
14%
—
congenital liver fibrosis —
19%
swelling of the face in the morning
14%
—
a history of organ transplantation —
19%
subcutaneous edema
14%
—
macrocephaly —
19%
eating ice
14%
—
history of liver surgery —
18%
stones in the bladder
14%
—
dryness —
18%
glomerulonephritis
24%
8%
adynamia —
18%
puffiness of the eyelids in the morning
14%
—
increased alt —
18%
no discharge
13%
—
cardiac cirrhosis of the liver —
18%
urine light
13%
—
expansion of the esophagus —
18%
thirst
13%
—
increased ast —
18%
brown urine
13%
—
diarrhea —
18%
altitude sickness
13%
—
liquid stool —
18%
chronic arthritis
13%
—
lower cholesterol —
18%
tuberculosis intoxication
13%
—
progressive supranuclear paralysis —
18%
is very sensitive
13%
—
neurological disorders —
18%
pulmonary edema
13%
—
dyslipidemia —
17%
chronic dysentery
13%
—
epilepsy in the morning —
17%
hypogammaglobulinemia
13%
—
chronic venous edema —
17%
nephropathy
28%
13%
damage to the nervous system —
17%
tuberculosis arthritis
12%
—
malabsorption —
17%
aslo is reduced
12%
—
hypertrophy of the left ventricle —
17%
kidney damage
12%
—
abdominal pain —
17%
lead poisoning
12%
—
stroke —
17%
systemic lupus erythematosus
12%
—
hepatoses —
17%
dysentery
12%
—
enteropathy —
17%
bacterial dysentery
12%
—
hepatosis fatty —
17%
intestinal colic
12%
—
congenital anomalies of the lower extremities —
17%
hypersthenuria
12%
—
liver atrophy —
17%
chronic enterocolitis
12%
—
kidney transplantation —
17%
cylindruria
12%
—
need for fats —
17%
osteoporosis
12%
—
liver dysfunction —
16%
amyloidosis of the kidneys
12%
—
abdominal swelling —
16%
syphilis
12%
—
calcification —
16%
azotemia
12%
—
polyneuropathy —
16%
diphtheria
11%
—
arrhythmia —
16%
chronic osteomyelitis
11%
—
cirrhosis of the liver —
16%
very pale
11%
—
cognitive disorders —
16%
tuberculosis of bones
11%
—
affective disorders —
16%
endocarditis
11%
—
suspicion —
16%
chilly
11%
—
blindness —
16%
kidney disease
27%
14%
effects of puberty —
16%
nephritic syndrome
11%
—
hypertrophy biliary tract —
16%
tuberculosis of the joints
11%
—
heart hypertrophy —
16%
sediment urine
21%
8%
muscle weakness —
16%
inflammation
21%
8%
limbs pain —
16%
hemorrhagic syndrome
11%
—
corneal opacity —
16%
liebman-sachs endocarditis
11%
—
violation of the stool —
16%
pale face
11%
—
muscular dystonia —
16%
lymphogranulomatosis
11%
—
early development —
16%
decrease in gamma globulins
10%
—
paranoia —
16%
fluid retention
10%
—
hemophagocytic syndrome —
16%
infectious colitis
10%
—
infantile —
16%
immunoglobulin a deficiency
10%
—
swelling of the legs —
16%
viral endocarditis
10%
—
chronic heart failure —
16%
amyloidosis
10%
—
venous congestion —
15%
malignant lymphoma
10%
—
anomalies of esophageal development —
15%
blisters
10%
—
progressive paralysis —
15%
bone necrosis
10%
—
abdominal pain after diarrhea —
15%
polyarthritis
10%
—
memory impairment —
15%
iron deficiency anemia
10%
—
nose nursing mom —
15%
oxalaturia
10%
—
angiopathy —
15%
colic
10%
—
greasy stools —
15%
osteopenia
10%
—
hypotension with weakness —
15%
hypochromia
10%
—
ataxia —
15%