|
OMIM |
Link |
Information
gain |
01 |
|
|
spondyloepiphyseal dysplasia tarda, autosomal recessive
|
[NCBI]
|
0.00224712
|
|
|
|
IGAN1
|
[NCBI]
|
0.00122186
|
|
|
|
GPS
|
[NCBI]
|
0.00122186
|
|
|
|
PF4
|
[NCBI]
|
0.000808575
|
|
|
|
B2M
|
[NCBI]
|
0.000348658
|
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
0.000152141
|
|
|
|
immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes
|
[NCBI]
|
0.000134642
|
|
|
|
HPA1
|
[NCBI]
|
0.000126907
|
|
|
|
membranoproliferative glomerulonephritis, x-linked
|
[NCBI]
|
0.000126907
|
|
|
|
complement factor i deficiency
|
[NCBI]
|
0.000106667
|
|
|
|
MKS1
|
[NCBI]
|
9.02824e-05
|
|
|
|
NEM3
|
[NCBI]
|
8.90247e-05
|
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
8.45992e-05
|
|
|
|
PFIC1
|
[NCBI]
|
8.17735e-05
|
|
|
|
HBB
|
[NCBI]
|
6.76466e-05
|
|
|
|
C3
|
[NCBI]
|
6.74398e-05
|
|
|
|
RA
|
[NCBI]
|
4.80915e-05
|
|
|
|
CEACAM5
|
[NCBI]
|
4.51468e-05
|
|
|
|
CHS
|
[NCBI]
|
4.40736e-05
|
|
|
|
PSG3
|
[NCBI]
|
2.63379e-05
|
|
|
|
AMY1A
|
[NCBI]
|
2.27807e-05
|
|
|
|
HPX
|
[NCBI]
|
1.96233e-05
|
|
|
|
GATA1
|
[NCBI]
|
1.90253e-05
|
|
|
|
complement component 2 deficiency
|
[NCBI]
|
1.83626e-05
|
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
1.77745e-05
|
|
|
|
C4B
|
[NCBI]
|
1.76644e-05
|
|
|
|
HP
|
[NCBI]
|
1.75618e-05
|
|
|
|
HEXA
|
[NCBI]
|
1.44455e-05
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
8.98087e-06
|
|
|
|
SERPINA6
|
[NCBI]
|
8.29485e-06
|
|
|
|
SLE
|
[NCBI]
|
8.12493e-06
|
|
|
|
CF
|
[NCBI]
|
7.44355e-06
|
|
|
|
GPI
|
[NCBI]
|
7.43465e-06
|
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
5.33378e-06
|
|
|
|
ALB
|
[NCBI]
|
4.7064e-06
|
|
|
|
TF
|
[NCBI]
|
3.16305e-06
|
|
|
|
G6PD
|
[NCBI]
|
1.8795e-06
|
|
|
|
ACHE
|
[NCBI]
|
1.6867e-07
|
|
|
|
AFP
|
[NCBI]
|
1.30111e-07
|
|
