Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 58% —
Register , to see more distinctive signs of diseases and studies — 71%
pseudoachondroplasia
55%
—
frequent otitis —
38%
nose eye fatigue
51%
—
enlargement of the spleen —
36%
milk intolerance
50%
—
macrocephaly —
36%
moody child
50%
—
enlargement of the liver and spleen —
35%
nose good
47%
—
night apnea —
34%
red blood vessels of the eyes
44%
—
otitis —
34%
motor anxiety
43%
—
apnea —
33%
lordosis
37%
—
enlarged liver —
33%
chondrodystrophy
37%
—
hydrocephalus —
33%
hypochondroplasia
33%
—
convulsions —
32%
x-shaped legs
31%
—
macular —
32%
stubbornness
45%
12%
chronic otitis —
31%
spina bifida
30%
—
mucopolysaccharidosis
22%
53%
flat back syndrome
29%
—
hepatosplenomegaly —
31%
thoracolumbar kyphosis
25%
—
umbilical hernia —
30%
spinal deviation
25%
—
coarsening of facial features —
29%
arthrosis of the knee joint
24%
—
hernia of the abdomen —
29%
anxiety
35%
9%
moderate condition —
28%
posterior costal hump
24%
—
delayed speech development —
28%
coxarthrosis
24%
—
heart failure —
26%
is not deformed
24%
—
angiopathy —
25%
deficit of stg
24%
—
rashes on the shoulders —
25%
torso
23%
—
pneumonia —
24%
arthrogryposis
23%
—
rashes on thighs —
24%
excess stg
23%
—
acute otitis —
24%
skew of blades
23%
—
contracture of the lower jaw —
24%
lumbar lordosis increased
22%
—
chronic tracheitis —
23%
crooked legs
42%
18%
epilepsy —
22%
ehlers - danlos syndrome
22%
—
mitral heart defects —
22%
tracheopesophageal fistula
22%
—
inguinal hernia —
22%
congenital anomalies of the lower extremities
22%
—
hearing impaired
13%
34%
shortening of legs
36%
12%
alpha-mannosidosis —
21%
congenital anomalies of the upper extremities
22%
—
corneal
11%
32%
o-shaped legs
22%
—
mongolian spot —
20%
skeletal deformity
34%
11%
up circulatory disorders —
20%
frequent colds
38%
15%
difficult to swallow —
20%
spondylolysis
20%
—
increased hairiness —
20%
calculating
20%
—
childhood diseases
10%
30%
position of the sacrum closer to horizontal
20%
—
macroglossia —
20%
spondylolisthesis
20%
—
epilepsy attacks —
19%
shoulder girdle skew
20%
—
otitis is viral —
19%
fistula of the anus
20%
—
viral pneumonia —
19%
motor activity
19%
—
epileptiform seizures —
19%
wedge - shaped vertebrae
19%
—
tingling of the fingertips —
19%
chondrodysplasia
19%
—
cardiomyopathy —
19%
harelip
19%
—
rashes on his legs —
19%
neurofibromatosis
19%
—
mental retardation —
19%
asymmetry
18%
—
clumsiness —
18%
surgical infections
18%
—
large child —
18%
perihepatitis
18%
—
swelling —
18%
angular hump
18%
—
destructive behavior —
18%
osteoarthritis of the spine
18%
—
clumsy —
18%
osteogenesis imperfecta
18%
—
pneumonia vomiting —
18%
myotonia
17%
—
often laryngotracheitis —
18%
brachydactyly
17%
—
mitral valve —
18%
wound postoperative
17%
—
choking on solid food —
18%
muscle atrophy
17%
—
diarrhea —
18%
stigmas of dysembriogenesis
17%
—
constantly swallows saliva —
18%
doubling of the kidney
17%
—
anomalies of language —
18%
congenital deafness
17%
—
mental retardation —
18%
bone fistula
17%
—
laryngotracheitis in children —
18%
syndactyly
17%
—
liquid stool —
18%
spinal abnormalities
17%
—
aspiration pneumonia —
18%
chest is flat
17%
—
tracheitis —
18%
conservative
17%
—
inguinal hernia in children —
18%
weakness of the ligaments
16%
—
hypertrophy of the tonsils —
18%
tension in the spine
16%
—
hearing loss in children —
18%
abnormalities of intestinal development
16%
—
thick bushy eyebrows —
18%
marfan syndrome
16%
—
tracheitis in a child —
17%
fistula
16%
—
hernia
14%
31%
kidney disease
16%
—
hair on the tongue —
17%
injury
16%
—
joints unstable —
17%
hydronephrosis
16%
—
chills in the afternoon —
17%
misalignment of pelvis
16%
—
eyelashes long —
17%
wet skin
16%
—
aggressive —
16%
forced situation
16%
—
visual impairment —
16%
age 4 years
15%
—
heart murmurs —
16%
position of the sacrum closer to the vertical
15%
—
compression myelopathy —
16%
weak joints
15%
—
pneumonia diarrhea —
16%
paralytic syndrome
15%
—
children's aphasia —
16%
make the main
15%
—
violation of the chair —
16%
noonan syndrome
14%
—
glaucoma —
16%
lumbalization
14%
—
laryngitis in children —
16%
pfoundler 's disease
14%
—
restless hands —
16%
movement in thoracic region is limited
14%
—
hyperactive —
16%
improvement from physical exertion
14%
—
tingling in the fingers —
16%
diastematomyelia
14%
—
rashes dry —
16%
holt-oram syndrome
14%
—
hearing loss after otitis —
16%
navel fistula
14%
—
No saliva —
16%
dystrophic myotonia
14%
—
umbilical hernia in children —
16%
sprengel 's disease
14%
—
dystrophy
8%
24%
spondyloepiphyseal dysplasia
14%
—
scoliosis in children —
15%
horse foot
14%
—
fidgety —
15%
morchio 's disease
14%
—
hydrocephalus in children —
15%
hormonal disorders
14%
—
temperature urticaria —
15%
incomplete bowel rotation
14%
—
increased intracranial pressure —
15%
gurler syndrome
14%
—
tingling in the fingers —
15%
werdnig-hoffman amyotrophy
14%
—
adenoids —
15%
peaked kyphosis
14%
—
wide shoulders —
15%
postoperative pain
14%
—
otitis media in children —
15%