|
1
|
(HPO:0001006)
|
Hypotrichosis |
Frequent [Orphanet]
|
|
|
|
219 / 7739
|
|
2
|
(HPO:0008207)
|
Primary adrenal insufficiency |
Very frequent [Orphanet]
|
|
|
|
26 / 7739
|
|
3
|
(HPO:0000820)
|
Abnormality of the thyroid gland |
Very frequent [Orphanet]
|
|
|
|
19 / 7739
|
|
4
|
(HPO:0100651)
|
Type I diabetes mellitus |
Very frequent [Orphanet]
|
|
|
|
44 / 7739
|
|
5
|
(HPO:0000829)
|
Hypoparathyroidism |
Frequent [Orphanet]
|
|
|
|
22 / 7739
|
|
6
|
(HPO:0001053)
|
Hypopigmented skin patches |
Frequent [Orphanet]
|
|
|
|
80 / 7739
|
|
7
|
(HPO:0000518)
|
Cataract |
|
|
|
|
454 / 7739
|
|
8
|
(HPO:0000585)
|
Band keratopathy |
|
|
|
|
8 / 7739
|
|
9
|
(HPO:0000821)
|
Hypothyroidism |
|
|
|
|
141 / 7739
|
|
10
|
(HPO:0000836)
|
Hyperthyroidism |
|
|
|
|
25 / 7739
|
|
11
|
(HPO:0001096)
|
Keratoconjunctivitis |
|
|
|
|
3 / 7739
|
|
12
|
(HPO:0001250)
|
Seizures |
|
|
|
|
1245 / 7739
|
|
13
|
(HPO:0001281)
|
Tetany |
|
|
|
|
20 / 7739
|
|
14
|
(HPO:0001394)
|
Cirrhosis |
|
|
|
|
102 / 7739
|
|
15
|
(HPO:0001596)
|
Alopecia |
|
|
|
|
162 / 7739
|
|
16
|
(HPO:0001738)
|
Exocrine pancreatic insufficiency |
|
|
|
|
23 / 7739
|
|
17
|
(HPO:0001746)
|
Asplenia |
|
|
|
|
19 / 7739
|
|
18
|
(HPO:0001891)
|
Iron deficiency anemia |
|
|
|
|
22 / 7739
|
|
19
|
(HPO:0002086)
|
Abnormality of the respiratory system |
|
|
|
|
17 / 7739
|
|
20
|
(HPO:0002570)
|
Steatorrhea |
|
|
|
|
31 / 7739
|
|
21
|
(HPO:0002728)
|
Chronic mucocutaneous candidiasis |
|
|
|
|
14 / 7739
|
|
22
|
(HPO:0003011)
|
Abnormality of the musculature |
Frequent [Orphanet]
|
|
|
|
47 / 7739
|
|
23
|
(HPO:0005978)
|
Type II diabetes mellitus |
|
|
|
|
68 / 7739
|
|
24
|
(HPO:0012115)
|
Hepatitis |
|
|
|
|
24 / 7739
|
|
25
|
(HPO:0100522)
|
Thymoma |
|
|
|
|
5 / 7739
|
|
26
|
(OMIM)
|
Candidal granuloma |
|
|
|
|
1 / 7739
|
|
27
|
(OMIM)
|
Thymic dysplasia |
|
|
|
|
1 / 7739
|
|
28
|
(OMIM)
|
Association of HLA-B8 |
|
|
|
|
1 / 7739
|
|
29
|
(HPO:0002843)
|
Abnormality of T cells |
|
|
|
|
7 / 7739
|
|
30
|
(HPO:0005352)
|
Severe T-cell immunodeficiency |
|
|
|
|
20 / 7739
|
|
31
|
(HPO:0005354)
|
Absent cellular immunity |
|
|
|
|
2 / 7739
|
|
32
|
(HPO:0005374)
|
Cellular immunodeficiency |
|
|
|
|
5 / 7739
|
|
33
|
(OMIM)
|
Adrenal failure |
|
|
|
|
2 / 7739
|
|
34
|
(OMIM)
|
Pernicious anemia |
|
|
|
|
3 / 7739
|
|
35
|
(OMIM)
|
Myxedema |
|
|
|
|
3 / 7739
|
|
36
|
(MedDRA:10023874)
|
Laryngitis |
|
|
|
|
2 / 7739
|
|
37
|
(OMIM)
|
Chronic pulmonary disease |
|
|
|
|
1 / 7739
|
|
38
|
(HPO:0200123)
|
Chronic hepatitis |
|
|
|
|
4 / 7739
|
|
39
|
(OMIM)
|
Splenic agenesis |
|
|
|
|
2 / 7739
|
|
40
|
(HPO:0008373)
|
Puberty and gonadal disorders |
Frequent [Orphanet]
|
|
|
|
156 / 7739
|