Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 48% —
Register , to see more distinctive signs of diseases and studies — 83%
kugelberg-velander amyotrophy
40%
—
corneal —
58%
muscle atrophy
31%
—
enlargement of the spleen —
58%
fasciculations
27%
—
enlargement of the liver and spleen —
57%
hoffmann 's perifolliculitis
26%
—
coarsening of facial features —
54%
werdnig-hoffman amyotrophy
24%
—
enlarged liver —
54%
becker's progressive muscular dystrophy
22%
—
hepatosplenomegaly —
53%
progressive erba-roth muscular dystrophy
21%
—
hearing impaired —
53%
tremor
21%
—
umbilical hernia —
50%
cramps in the hips
21%
—
hernia of the abdomen —
48%
weakness in the shoulder
19%
—
hernia —
48%
twitching of the hands
19%
—
compression of the spinal cord —
47%
muscular dystrophy
19%
—
lumbar kyphosis —
46%
motor activity
19%
—
curvature of the spine
15%
59%
weakness of the muscles of the hands
19%
—
low —
43%
weakness in the hip
18%
—
neck is short —
42%
weakness in the hands
18%
—
gurler syndrome —
41%
myopathies
18%
—
pfoundler 's disease —
41%
cramps of the hands
17%
—
frequent otitis —
41%
knee reflex negative
17%
—
stooped
15%
55%
spastic paralysis
17%
—
hump
15%
55%
weakness in the arms and legs
17%
—
tension in the face —
40%
better evening
16%
—
lags behind in the development —
40%
cerebral palsy
16%
—
otitis —
40%
misalignment of pelvis
16%
—
stiffness in the joints
6%
46%
tremor of the hands and tongue
15%
—
glaucoma —
39%
weakness of the neck muscles
15%
—
chest deformity
13%
52%
tics
14%
—
joint deformation
15%
53%
oppenheim syndrome
14%
—
hunter syndrome —
37%
osteopenia
14%
—
arthropathy
10%
47%
sits sideways
14%
—
crooked legs
12%
48%
protein-energy deficiency
14%
—
sanfilippo syndrome —
36%
twitching of the leg muscles
14%
—
morchio 's disease —
34%
hematomyelia
14%
—
visual impairment —
34%
osteoporosis
14%
—
chronic otitis —
33%
congenital myopathies
14%
—
cognitive disorders —
33%
duck gait
14%
—
hydrocephalus —
33%
muscle fatigue
14%
—
mental retardation —
33%
protein c deficiency
14%
—
alpha-mannosidosis —
33%
inflammatory myopathy
13%
—
clumsiness —
33%
patient is motionless
13%
—
kyphosis scoliosis
14%
47%
fussiness and anxiety
13%
—
scarring
10%
42%
weakness in the neck
13%
—
cardiac disorder
11%
42%
tremor in the legs
13%
—
tendon compaction —
30%
perihepatitis
13%
—
s eyes cloudy —
30%
atrophoderma
13%
—
scoliosis
16%
46%
amyotrophic lateral sclerosis
13%
—
deformations of the feet
13%
43%
bone fracture
13%
—
hearing loss in children —
30%
glycogenoses
13%
—
trunk is shortened —
30%
ganglioneuritis
13%
—
epilepsy —
29%
tired when walking
13%
—
growth retardation —
29%
tremor of the hands
13%
—
her hair is hard —
29%
tremor of the hands
13%
—
pigmented glaucoma —
28%
striae
13%
—
epiphyseal dysplasia —
28%
sticks out the tongue
13%
—
weakness of the bladder —
28%
trembling tongue
13%
—
spinal canal stenosis —
28%
problems with the father
12%
—
macular —
28%
terminal states
12%
—
thoracolumbar kyphosis —
28%
better from movement
12%
—
spondylopathy
15%
43%
flaccid paralysis syndrome
12%
—
muscle tension
7%
35%
marfan syndrome
12%
—
mental retardation —
27%
fruits when running worse
12%
—
swelling —
27%
myelitis
12%
—
disorder of violation of bodily form —
27%
type of breathing chest
12%
—
contracture of the lower jaw —
27%
sluggish baby
12%
—
restless hands —
27%
independent
12%
—
hypertrophy of the tonsils —
27%
hypercapnia
12%
—
wide shoulders —
27%
intramedullary tumors of the spinal cord
12%
—
adenoids —
27%
weakness in the lower back
12%
—
macrocephaly —
26%
worse from pressure
12%
—
nose large eyes —
26%
worse from increased pressure
12%
—
periods of exacerbation —
26%
hip dislocation
12%
—
chills in the afternoon —
26%
quickly gets tired
11%
—
deafness —
26%
fibrillar twitching of tongue
11%
—
calve's disease —
26%
suspicion
11%
—
chronic respiratory failure —
26%
doubts
11%
—
frequent runny —
25%
paranoia
11%
—
macroglossia —
25%
tame child
11%
—
deformation of the skull —
25%
to increase the mammary glands
11%
—
sunken eyes —
25%
is better pain in the shower
11%
—
osteochondropathy —
25%
is not deformed
11%
—
constantly swallows saliva —
25%
slouching sitting
11%
—
heart failure
6%
31%
no pharyngeal reflex
11%
—
night apnea
14%
39%
fasting
11%
—
plump lips —
25%
of medica matter
11%
—
intellectual disabilities in children —
24%
roth's disease
11%
—
epilepsy attacks —
24%
head tilted
11%
—
shortening of legs —
24%
gangrene
10%
—
rashes dry —
24%
can't sit
10%
—
smart baby —
24%
hypoglycemia
10%
—
polyarthritis —
24%
increased fatigue
10%
—
swelling of the tongue —
24%
dysfunction of the left lung
10%
—
bone deformation
9%
33%
plays toys
10%
—
anomalies of language —
23%
consultation of a gastroenterologist
10%
—
No saliva —
23%
severe pain in the lower back
10%
—
shortening of limbs —
23%
acute nasopharyngitis runny
10%
—
temperature urticaria —
23%
delayed reaction
10%
—
increased hairiness —
23%
stretching
10%
—
big nose —
23%
cold weakness
10%
—
worries about the work —
23%
can not hold his head
10%
—
destructive behavior —
23%
patient experiencing no
10%
—
ventriculitis —
23%