Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 28% —
Register , to see more distinctive signs of diseases and studies — 74%
hemoglobinuria
26%
—
mucopolysaccharidosis —
58%
dark urine
23%
—
frequent otitis —
37%
hemolytic anemia
21%
—
macrocephaly —
37%
hypersplenism
18%
—
hearing impaired —
35%
erythrocytic anemia
18%
—
otitis —
35%
anemia
17%
—
curvature of the spine —
35%
urine color dark yellow
17%
—
night apnea —
34%
hemolytic anemia in children
17%
—
hydrocephalus —
34%
paroxysmal nocturnal hemoglobinuria
16%
—
apnea —
34%
hyperbilirubinemia
15%
—
retinal dystrophy —
33%
jaundice
15%
—
convulsions —
33%
aplastic anemia
14%
—
corneal opacity —
33%
anemia, unspecified
14%
—
respiratory arrest in a dream —
32%
myelodysplastic syndrome
14%
—
chronic otitis —
32%
pregnancy
25%
9%
coarsening of facial features —
32%
decreased vitamin b9
14%
—
hernia —
32%
gallbladder stones
14%
—
hump —
32%
dysfunction of the gallbladder
13%
—
umbilical hernia —
31%
allgrove syndrome
13%
—
kyphosis scoliosis —
30%
hemolytic disease of newborns
13%
—
moderate condition —
29%
yellow skin color
12%
—
neurological disorders —
29%
hemoglobin increased
12%
—
delayed speech development —
28%
kidney disease
12%
—
hernia of the abdomen —
28%
beriberi
12%
—
joint diseases
4%
31%
minkowski-shoffar disease
12%
—
children's speech —
27%
the skin is dark
12%
—
scoliosis —
26%
hypertrophy biliary tract
12%
—
heart failure —
26%
oncology
12%
—
there is heart failure —
26%
erythropenia
11%
—
enlargement of the liver and spleen
11%
37%
portal vein thrombosis
11%
—
bone deformation
8%
34%
splenectomy
11%
—
lags behind in the development —
26%
reticulocytosis
11%
—
rashes on thighs —
25%
anuria
11%
—
neck is short —
25%
monocytic ehrlichiosis
11%
—
acute otitis —
25%
pulmonary hypertension
11%
—
rashes on the shoulders —
25%
cholelithiasis in children
11%
—
hepatosplenomegaly
7%
32%
rhesus conflict
11%
—
dystrophy —
25%
yellowness of mucous membranes
11%
—
pneumonia —
25%
erythrocytosis
11%
—
stunting —
24%
hemoglobinopathies
11%
—
alpha-mannosidosis —
24%
thalassemia
10%
—
contracture of the lower jaw —
24%
oliguria
10%
—
spondylopathy —
24%
pink urine
10%
—
heart dysfunction
5%
29%
decrease in indirect bilirubin
10%
—
enlarged liver
10%
34%
increased ldh
10%
—
chronic tracheitis —
23%
loves black
10%
—
inguinal hernia —
23%
granulocytic ehrlichiosis
10%
—
enlargement of the spleen
14%
37%
immune hemolytic anemia
10%
—
polyarthritis —
23%
budd—chiari syndrome
10%
—
2 children —
22%
helminths
9%
—
rashes on the hands and feet —
22%
intoxication
9%
—
height is low —
22%
chronic kidney disease
9%
—
epilepsy —
22%
diseases of infants
9%
—
mitral heart defects —
22%
bilirubinuria
9%
—
contracture —
22%
acute venous thrombosis
9%
—
childhood diseases
8%
30%
fever weakness
9%
—
increased hairiness —
21%
transferrin increase
9%
—
stiffness in the joints —
21%
leukemia
9%
—
joint deformation
4%
25%
apex systolic murmur
9%
—
contractures of the joints —
21%
tartar
9%
—
macroglossia —
21%
digestive weakness
8%
—
up circulatory disorders —
21%
monocytopenia
8%
—
constantly swallows saliva —
20%
interruptions in the work of the heart
8%
—
can't chew —
20%
consequences of childbirth
8%
—
viral pneumonia —
20%
curvature of the nose
8%
—
thick bushy eyebrows —
20%
chronic condition
8%
—
absences —
20%
anemia in children
8%
—
tingling of the fingertips —
20%
number of births increased
8%
—
viral otitis media —
20%
general weakness
8%
—
rashes on the hands —
20%
myeloma
8%
—
metabolic disorder —
20%
heaviness in the epigastric
8%
—
tracheitis —
20%
very pale
8%
—
hypertrophy of the tonsils —
20%
skin color
8%
—
inflammation
8%
28%
bone metastasis
8%
—
rashes on his legs —
20%
hemochromatosis
8%
—
cardiomyopathy —
19%
vitamin b12 reduction2
8%
—
diarrhea with colds —
19%
plaque on the teeth
8%
—
epilepsy attacks —
19%
hyperchromia
8%
—
liquid stool —
19%
black discharge
8%
—
aspiration pneumonia —
19%
cholecystectomy
8%
—
chest deformity —
19%
anemia during pregnancy
8%
—
compression of the spinal cord —
19%
lesion increased
8%
—
mongolian spot —
19%
sickle cell anemia
8%
—
delay of mental development —
19%
swelling during pregnancy
8%
—
diarrhea —
19%
choleretic
8%
—
mitral valve insufficiency —
19%
porphyria
8%
—
early development —
19%
cylindruria
8%
—
spinal canal stenosis —
19%
lymphocytic
8%
—
arthritis —
19%
malaria
8%
—
pneumonia vomiting —
18%
hypobilirubinemia
8%
—
hearing loss in children —
18%
volume of gallbladder is increased
8%
—
mental retardation —
18%
state of exacerbation
8%
—
destructive behavior —
18%
muscular dystonia
8%
—
No saliva —
18%
peripheral artery thrombosis
7%
—
hair on the tongue —
18%
myelofibrosis
7%
—
laryngotracheitis in children —
18%
abdominal pain
7%
—
large child —
18%
solid tumors
7%
—
clumsiness —
18%
iron deficiency anemia
7%
—
epiphyseal dysplasia —
18%
abdominal discomfort
7%
—
choking on solid food —
18%
kidney damage
7%
—
anomalies of tongue —
18%