Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 66% —
Register , to see more distinctive signs of diseases and studies — 100%
throat hurts
44%
—
kalman syndrome —
86%
pendred syndrome
42%
—
dystrophy —
83%
hearing loss
38%
—
hypogonadism —
81%
hearing loss in children
35%
—
photophobia —
78%
waardenburg syndrome
30%
—
ahlstrom syndrome —
77%
neuritis of the auditory nerve
29%
—
dilated cardiomyopathy —
77%
stickler syndrome
27%
—
testicular atrophy —
77%
children's speech
27%
—
metabolic syndrome —
76%
speech slurred
27%
—
thyroid atrophy —
73%
delayed speech development
23%
—
pancreatic atrophy —
73%
neuritis
23%
—
black acanthosis —
73%
neuralgia
23%
—
increased uric acid —
71%
air sickness
22%
—
cardiodilation —
70%
childhood diseases
22%
—
obesity —
68%
alalia
21%
—
type 2 diabetes mellitus —
67%
limited vocabulary
21%
—
diabetes mellitus —
63%
early development
21%
—
uric acid of urine is elevated —
63%
motion sickness in transport
20%
—
ovarian hypoplasia —
62%
lags behind in the development
20%
—
cardiomyopathy —
62%
bright eyes
20%
—
defects of dentition —
60%
psoriasis
19%
—
polycystic ovary syndrome pcos —
59%
hyperkeratosis
18%
—
blurred vision —
59%
Follows the rules
18%
—
testicular cyst —
59%
deafness
82%
63%
weight change —
59%
angiopathy of the retina
17%
—
proteinuria —
58%
thyroid diseases
16%
—
retinitis pigmentosa —
58%
problems with studying
15%
—
ovarian endometriosis —
58%
madness
15%
—
heart dysfunction —
58%
delirium
15%
—
hormonal disorders
14%
71%
responsible
15%
—
angioplasty —
57%
confusion of consciousness
15%
—
uterine hypoplasia —
57%
angiopathy
13%
—
thyroid cyst —
57%
stage of recovery
13%
—
glycohemoglobin increased —
56%
recovery period
13%
—
nephropathy —
56%
skin problems
12%
—
retinal atrophy —
56%
hearing impaired
100%
91%
primary amenorrhea —
56%
blood diseases —
55%
congenital hypothyroidism —
54%
visual impairment —
54%
brachydactyly —
54%
hirsutism —
53%
increased triglycerides —
53%
polycystic ovaries —
53%
uterine appendages are increase —
52%
in the family diabetes —
52%
uterine cyst —
52%
underdevelopment
15%
67%
cryptorchidism —
52%
impaired glucose tolerance —
51%
skin dystrophy —
50%
hypertension —
50%
endometriosis —
50%
ovarian cysts —
50%
chorioretinitis —
50%
enlargement of the uterus —
50%
heart transplantation —
49%
eats often —
49%
increased hairiness —
49%
baldness —
49%
hepatosis fatty —
48%
can't hold urine —
48%
lack of menstruation —
48%
deformity of fingers —
47%
hepatoses —
47%
ovarian dysfunction —
47%
polycystic —
47%
nystagmus —
47%
heart disease in the genus —
47%
liver atrophy —
47%
insulin deficiency —
47%
hyperpigmentation —
47%
urinary incontinence —
47%
hemoglobin increased —
46%
skeletal deformity —
46%
hepatosplenomegaly —
46%
pancreatopathy —
45%
hair loss —
45%
enlargement of the liver and spleen —
44%
cystic fibrosis —
44%
type 1 diabetes mellitus —
44%
enlargement of the spleen —
43%
increased appetite —
43%
hypoglycemia —
43%
increased cholesterol —
43%
decreased intelligence —
43%
hyperlipidemia —
43%
sensorineural
27%
69%
curvature of the spine —
42%
brown spots on the skin —
42%
brown pigmentation after rashes —
42%
the skin is dark —
42%
hyperglycemia —
42%
nervousness —
41%
enlargement of the heart —
41%
appendages of the uterus —
41%
hypothyroidism —
41%
little urine —
41%
impaired uterine function —
41%
oily skin —
40%
enlarged liver —
40%
protein with increased —
39%
protein c deficiency —
39%
overweight —
38%
family man —
38%
a history of organ transplantation —
38%
there is heart failure —
37%
heart failure —
37%
female pelvic organs —
37%
there are no complaints —
33%
patient's condition —
31%
inflammation
17%
31%
hereditary hearing loss
56%
65%