Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 83% 22%
Register , to see more distinctive signs of diseases and studies — 58%
enlargement of the spleen
58%
—
pseudoachondroplasia —
55%
enlargement of the liver and spleen
57%
—
nose eye fatigue —
51%
enlarged liver
54%
—
milk intolerance —
50%
hepatosplenomegaly
53%
—
moody child —
50%
umbilical hernia
50%
—
nose good —
47%
hernia of the abdomen
48%
—
red blood vessels of the eyes —
44%
corneal
58%
11%
motor anxiety —
43%
frequent otitis
41%
—
chondrodystrophy —
37%
otitis
40%
—
stubbornness
10%
45%
tension in the face
40%
—
hypochondroplasia —
33%
glaucoma
39%
—
spina bifida —
30%
night apnea
39%
—
flat back syndrome —
29%
hearing impaired
53%
13%
spinal deviation —
25%
hunter syndrome
37%
—
arthrosis of the knee joint —
24%
coarsening of facial features
37%
—
is not deformed —
24%
apnea
37%
—
posterior costal hump —
24%
muscle tension
36%
—
coxarthrosis —
24%
sanfilippo syndrome
36%
—
torso —
23%
visual impairment
34%
—
arthrogryposis —
23%
clumsiness
33%
—
skew of blades —
23%
compression of the spinal cord
47%
12%
excess stg —
23%
alpha-mannosidosis
33%
—
ehlers - danlos syndrome —
22%
chronic otitis
33%
—
lumbar lordosis increased —
22%
mental retardation
33%
—
tracheopesophageal fistula —
22%
hydrocephalus
33%
—
o-shaped legs —
22%
stiffness in the joints
46%
12%
congenital anomalies of the lower extremities —
22%
hernia
48%
14%
congenital anomalies of the upper extremities —
22%
heart failure
31%
—
position of the sacrum closer to horizontal —
20%
childhood diseases
43%
10%
spondylolisthesis —
20%
stooped
55%
23%
calculating —
20%
hump
55%
23%
fistula of the anus —
20%
tendon compaction
30%
—
spondylolysis —
20%
hearing loss in children
30%
—
shoulder girdle skew —
20%
aspiration pneumonia
29%
—
motor activity —
19%
her hair is hard
29%
—
neurofibromatosis —
19%
scarring
43%
12%
chondrodysplasia —
19%
epilepsy
29%
—
harelip —
19%
pigmented glaucoma
28%
—
wedge - shaped vertebrae —
19%
mental retardation
28%
—
osteogenesis imperfecta —
18%
macular
28%
—
x-shaped legs
13%
31%
weakness of the bladder
28%
—
asymmetry —
18%
compression myelopathy
28%
—
perihepatitis —
18%
pneumonia vomiting
28%
—
osteoarthritis of the spine —
18%
hypertrophy of the tonsils
27%
—
angular hump —
18%
contracture of the lower jaw
27%
—
spinal abnormalities —
17%
restless hands
27%
—
chest is flat —
17%
wide shoulders
27%
—
congenital deafness —
17%
neck is short
42%
13%
myotonia —
17%
swelling
27%
—
muscle atrophy —
17%
chest deformity
52%
23%
syndactyly —
17%
joints unstable
27%
—
stigmas of dysembriogenesis —
17%
convulsions
27%
—
brachydactyly —
17%
angiopathy
27%
—
conservative —
17%
adenoids
27%
—
wound postoperative —
17%
macrocephaly
26%
—
doubling of the kidney —
17%
up circulatory disorders
26%
—
bone fistula —
17%
chills in the afternoon
26%
—
anxiety
18%
35%
respiratory insufficiency
26%
—
misalignment of pelvis —
16%
periods of exacerbation
26%
—
abnormalities of intestinal development —
16%
chronic respiratory failure
26%
—
hydronephrosis —
16%
pfoundler 's disease
41%
14%
marfan syndrome —
16%
swelling of the tongue
25%
—
wet skin —
16%
plump lips
25%
—
forced situation —
16%
constantly swallows saliva
25%
—
kidney disease —
16%
macroglossia
25%
—
weakness of the ligaments —
16%
frequent runny
25%
—
lordosis
21%
37%
difficult to swallow
25%
—
fistula —
16%
sunken eyes
25%
—
paralytic syndrome —
15%
pneumonia
25%
—
position of the sacrum closer to the vertical —
15%
gurler syndrome
41%
14%
make the main —
15%
heart hypertrophy
24%
—
age 4 years —
15%
deformations of the feet
44%
18%
incomplete bowel rotation —
14%
epilepsy attacks
24%
—
postoperative pain —
14%
rashes dry
24%
—
dystrophic myotonia —
14%
flat feet
24%
—
spondyloepiphyseal dysplasia —
14%
respiratory arrest in a dream
24%
—
sprengel 's disease —
14%
ones weakness in the leg muscles
24%
—
holt-oram syndrome —
14%
has been experiencing
23%
—
oncology —
14%
destructive behavior
23%
—
scoliotic deformity to the left —
14%
No saliva
23%
—
lumbalization —
14%
delayed speech development
23%
—
soft hair —
14%
vomiting
23%
—
intensive physical load —
14%
anomalies of language
23%
—
navel fistula —
14%
worries about the work
23%
—
hormonal disorders —
14%
increased hairiness
23%
—
werdnig-hoffman amyotrophy —
14%
temperature urticaria
23%
—
peaked kyphosis —
14%
cardiac disorder
42%
17%
movement in thoracic region is limited —
14%
big nose
23%
—
sacralization —
14%
ventriculitis
23%
—
noonan syndrome —
14%
shroud
22%
—
improvement from physical exertion —
14%
cognitive disorders
33%
9%
diastematomyelia —
14%
curvature of the spine
59%
35%
russi-levy syndrome —
14%
blurred vision
22%
—
frequent colds
24%
38%
acute otitis
22%
—
horse foot —
14%
lags behind in the development
40%
16%
variable symptoms —
13%
frequent antibiotics
22%
—
kidney agenesis —
13%
vomiting at high temperature
22%
—
stenosis of the mouth of the pulmonary artery —
13%
muscle weakness
22%
—
facial hair growth —
13%
tonsillitis
22%
—
histiocytosis x —
13%
moderate condition
21%
—
stiffness hip joints —
13%