1
|
(HPO:0000403)
|
Recurrent otitis media |
|
|
|
|
61 / 7739
|
2
|
(HPO:0001508)
|
Failure to thrive |
|
|
|
|
454 / 7739
|
3
|
(HPO:0001875)
|
Neutropenia |
rare [HPO:skoehler]
|
|
|
|
83 / 7739
|
4
|
(HPO:0002014)
|
Diarrhea |
|
|
|
|
225 / 7739
|
5
|
(HPO:0002718)
|
Recurrent bacterial infections |
|
|
|
|
75 / 7739
|
6
|
(HPO:0002837)
|
Recurrent bronchitis |
|
|
|
|
21 / 7739
|
7
|
(HPO:0004432)
|
Agammaglobulinemia |
|
|
|
|
17 / 7739
|
8
|
(HPO:0002205)
|
Recurrent respiratory infections |
|
|
|
|
254 / 7739
|
9
|
(MedDRA:10014866)
|
Enteritis |
|
|
|
|
2 / 7739
|
10
|
(OMIM)
|
Absent or severely reduced numbers of B cells |
|
|
|
|
5 / 7739
|
11
|
(OMIM)
|
Developmental arrest of B cells at the pre-B to pro-B cell transition stage |
|
|
|
|
1 / 7739
|
12
|
(OMIM)
|
Inability to mount antibody response to antigen |
|
|
|
|
4 / 7739
|
13
|
(OMIM)
|
Normal numbers and function of T cells |
|
|
|
|
4 / 7739
|
14
|
(OMIM)
|
Absence of lymph nodes (in 1 patient) |
|
|
|
|
1 / 7739
|
15
|
(MedDRA:10012503)
|
Dermatomyositis |
|
|
|
|
2 / 7739
|
16
|
(OMIM)
|
Hypogammaglobulinemia, profound |
|
|
|
|
5 / 7739
|
17
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|