|
OMIM |
Link |
Information gain |
01 |
|
ADA
|
[NCBI]
|
0.00405502
|
|
|
bare lymphocyte syndrome, type ii
|
[NCBI]
|
0.00247919
|
|
|
SCIDX1
|
[NCBI]
|
0.00244679
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
0.001706
|
|
|
severe combined immunodeficiency with sensitivity to ionizing radiation
|
[NCBI]
|
0.00111698
|
|
|
IL2RG
|
[NCBI]
|
0.00109401
|
|
|
PN
|
[NCBI]
|
0.00107364
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive
|
[NCBI]
|
0.000879195
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.000847142
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative
|
[NCBI]
|
0.000629213
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive
|
[NCBI]
|
0.000629213
|
|
|
JAK3
|
[NCBI]
|
0.000603872
|
|
|
RFX5
|
[NCBI]
|
0.000396131
|
|
|
DCLRE1C
|
[NCBI]
|
0.000362885
|
|
|
omenn syndrome
|
[NCBI]
|
0.000346885
|
|
|
RAG1
|
[NCBI]
|
0.000296479
|
|
|
RA
|
[NCBI]
|
0.000276351
|
|
|
RAG2
|
[NCBI]
|
0.000264648
|
|
|
IL7R
|
[NCBI]
|
0.000257218
|
|
|
LMO2
|
[NCBI]
|
0.000240061
|
|
|
SLE
|
[NCBI]
|
0.000228945
|
|
|
PRKDC
|
[NCBI]
|
0.000217393
|
|
|
RFXAP
|
[NCBI]
|
0.000205678
|
|
|
bare lymphocyte syndrome, type i
|
[NCBI]
|
0.000164375
|
|
|
RFXANK
|
[NCBI]
|
0.000162064
|
|
|
MHC2TA
|
[NCBI]
|
0.000138624
|
|
|
NP
|
[NCBI]
|
0.000137532
|
|
|
HHS
|
[NCBI]
|
0.000116498
|
|
|
PTPRC
|
[NCBI]
|
0.000113332
|
|
|
alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity
|
[NCBI]
|
0.000104577
|
|
|
severe combined immunodeficiency, atypical
|
[NCBI]
|
0.000104577
|
|
|
CD3D
|
[NCBI]
|
0.000102743
|
|
|
ZAP70
|
[NCBI]
|
8.56409e-05
|
|
|
HIGM1
|
[NCBI]
|
8.31671e-05
|
|
|
CF
|
[NCBI]
|
8.25424e-05
|
|
|
combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia
|
[NCBI]
|
8.21298e-05
|
|
|
t-cell immunodeficiency, congenital alopecia, and nail dystrophy
|
[NCBI]
|
8.21298e-05
|
|
|
ABSD
|
[NCBI]
|
8.21298e-05
|
|
|
WAS
|
[NCBI]
|
8.09029e-05
|
|
|
CIDX
|
[NCBI]
|
7.36732e-05
|
|
|
TNF
|
[NCBI]
|
6.67647e-05
|
|
|
CHS
|
[NCBI]
|
6.63163e-05
|
|
|
RFX1
|
[NCBI]
|
6.51141e-05
|
|
|
CEBPD
|
[NCBI]
|
6.51141e-05
|
|
|
TMEM142C
|
[NCBI]
|
6.51141e-05
|
|
|
TMEM142A
|
[NCBI]
|
6.51141e-05
|
|
|
TMEM142B
|
[NCBI]
|
6.51141e-05
|
|
|
CHH
|
[NCBI]
|
6.28953e-05
|
|
|
NN
|
[NCBI]
|
5.81925e-05
|
|
|
TAPBP
|
[NCBI]
|
5.13476e-05
|
|
|
FOXN1
|
[NCBI]
|
4.61603e-05
|
|
|
IL21R
|
[NCBI]
|
4.61603e-05
|
|
|
AT
|
[NCBI]
|
4.53171e-05
|
|
|
IL2RB
|
[NCBI]
|
4.27967e-05
|
|
|
VEGF
|
[NCBI]
|
4.23919e-05
|
|
|
SYK
|
[NCBI]
|
4.02991e-05
|
|
|
TAP1
|
[NCBI]
|
3.83117e-05
|
|
|
CD3E
|
[NCBI]
|
3.83117e-05
|
|
|
NFATC1
|
[NCBI]
|
3.52506e-05
|
|
|
LCK
|
[NCBI]
|
3.29263e-05
|
|
|
immunodeficiency-centromeric instability-facial anomalies syndrome
|
[NCBI]
|
3.22851e-05
|
|
|
TNFRSF13B
|
[NCBI]
|
3.19447e-05
|
|
|
LIG4
|
[NCBI]
|
3.19447e-05
|
|
|
IFNGR1
|
[NCBI]
|
2.75346e-05
|
|
|
IL2RA
|
[NCBI]
|
2.64253e-05
|
|
|
DKC1
|
[NCBI]
|
2.59161e-05
|
|
|
CHM
|
[NCBI]
|
2.52066e-05
|
|
|
NBS1
|
[NCBI]
|
2.26118e-05
|
|
|
COL17A1
|
[NCBI]
|
2.1625e-05
|
|
|
SH2D1A
|
[NCBI]
|
1.84969e-05
|
|
|
FOXP3
|
[NCBI]
|
1.72693e-05
|
|
|
WAS
|
[NCBI]
|
1.6896e-05
|
|
|
IL4
|
[NCBI]
|
1.55477e-05
|
|
|
ALPS
|
[NCBI]
|
1.55272e-05
|
|
|
KITLG
|
[NCBI]
|
1.50931e-05
|
|
|
PCNA
|
[NCBI]
|
1.4614e-05
|
|
|
BTK
|
[NCBI]
|
1.12009e-05
|
|
|
EV
|
[NCBI]
|
1.06752e-05
|
|
|
GFAP
|
[NCBI]
|
9.83386e-06
|
|
|
DGS
|
[NCBI]
|
8.67493e-06
|
|
|
STAT3
|
[NCBI]
|
4.62751e-06
|
|
|
CJD
|
[NCBI]
|
3.12788e-06
|
|
|
IL2
|
[NCBI]
|
2.87276e-06
|
|
|
CVID
|
[NCBI]
|
2.50193e-06
|
|
|
SLC6A3
|
[NCBI]
|
2.36213e-06
|
|
|
ACHE
|
[NCBI]
|
2.32922e-06
|
|
|
TH
|
[NCBI]
|
2.28979e-06
|
|
|
VIP
|
[NCBI]
|
5.29924e-07
|
|
|
PTHLH
|
[NCBI]
|
4.70331e-07
|
|
|
TNFSF6
|
[NCBI]
|
3.86569e-07
|
|