|
OMIM |
Link |
Information gain |
01 |
|
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|
[NCBI]
|
0.00276189
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.00151158
|
|
|
MAFD1
|
[NCBI]
|
0.00105379
|
|
|
ADA
|
[NCBI]
|
0.000933564
|
|
|
NT5C
|
[NCBI]
|
0.000234583
|
|
|
omenn syndrome
|
[NCBI]
|
0.000230099
|
|
|
syringomas, multiple
|
[NCBI]
|
0.000146557
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
5.37368e-05
|
|
|
NT5C2
|
[NCBI]
|
4.40199e-05
|
|
|
BPNT1
|
[NCBI]
|
4.40199e-05
|
|
|
BL
|
[NCBI]
|
3.79943e-05
|
|
|
BTK
|
[NCBI]
|
3.77469e-05
|
|
|
MUC15
|
[NCBI]
|
3.65978e-05
|
|
|
NT5E
|
[NCBI]
|
3.19791e-05
|
|
|
SLE
|
[NCBI]
|
3.06745e-05
|
|
|
NT5C3
|
[NCBI]
|
2.72195e-05
|
|
|
DCK
|
[NCBI]
|
2.70922e-05
|
|
|
APRT
|
[NCBI]
|
2.46193e-05
|
|
|
G6PD
|
[NCBI]
|
2.02054e-05
|
|
|
PDE6B
|
[NCBI]
|
1.91704e-05
|
|
|
CD
|
[NCBI]
|
1.64781e-05
|
|
|
ACHE
|
[NCBI]
|
1.10435e-05
|
|
|
RA
|
[NCBI]
|
8.72408e-06
|
|
|
MG
|
[NCBI]
|
4.9465e-06
|
|
|
ALB
|
[NCBI]
|
4.94263e-06
|
|
|
DHFR
|
[NCBI]
|
1.77958e-06
|
|
|
CFTR
|
[NCBI]
|
8.49389e-07
|
|
|
EGF
|
[NCBI]
|
7.68724e-07
|
|
|
CHAT
|
[NCBI]
|
6.03853e-07
|
|
|
CEACAM5
|
[NCBI]
|
8.08535e-08
|
|