|
OMIM |
Link |
Information gain |
01 |
|
CF
|
[NCBI]
|
0.00681326
|
|
|
IGAD1
|
[NCBI]
|
0.00212912
|
|
|
opsismodysplasia
|
[NCBI]
|
0.00074746
|
|
|
neutrophilic dermatosis, acute febrile
|
[NCBI]
|
0.000564232
|
|
|
RA
|
[NCBI]
|
0.000505863
|
|
|
IGAN1
|
[NCBI]
|
0.000464919
|
|
|
ATD1
|
[NCBI]
|
0.000425595
|
|
|
SLE
|
[NCBI]
|
0.00042358
|
|
|
CVID
|
[NCBI]
|
0.000319996
|
|
|
PCD
|
[NCBI]
|
0.000313371
|
|
|
RNASE3
|
[NCBI]
|
0.000221866
|
|
|
MBL2
|
[NCBI]
|
0.000216526
|
|
|
young syndrome
|
[NCBI]
|
0.000198527
|
|
|
MPO
|
[NCBI]
|
0.000154483
|
|
|
kartagener syndrome
|
[NCBI]
|
0.000143154
|
|
|
retinitis pigmentosa, x-linked, with recurrent respiratory infections
|
[NCBI]
|
0.00012943
|
|
|
MRXSL
|
[NCBI]
|
0.000122126
|
|
|
CFTR
|
[NCBI]
|
0.000113517
|
|
|
GBS
|
[NCBI]
|
9.97677e-05
|
|
|
thoracic dysostosis, isolated
|
[NCBI]
|
9.18797e-05
|
|
|
gamma-a-globulin, defect in assembly of
|
[NCBI]
|
9.18797e-05
|
|
|
lymphoid system deterioration, progressive
|
[NCBI]
|
9.18797e-05
|
|
|
granulomatous disease due to combined cellular and humoral immune defects
|
[NCBI]
|
9.18797e-05
|
|
|
kawasaki disease
|
[NCBI]
|
8.68711e-05
|
|
|
tracheal antimicrobial peptide
|
[NCBI]
|
7.52968e-05
|
|
|
UCMD
|
[NCBI]
|
7.34457e-05
|
|
|
HNA
|
[NCBI]
|
7.34457e-05
|
|
|
tracheobronchomegaly
|
[NCBI]
|
6.94631e-05
|
|
|
RPGR
|
[NCBI]
|
6.52269e-05
|
|
|
ceroid storage disease
|
[NCBI]
|
6.10369e-05
|
|
|
pulmonary hypertension, primary, autosomal recessive
|
[NCBI]
|
6.10369e-05
|
|
|
SLPI
|
[NCBI]
|
5.64941e-05
|
|
|
TNFRSF4
|
[NCBI]
|
5.63247e-05
|
|
|
ciliary discoordination due to random ciliary orientation
|
[NCBI]
|
5.55846e-05
|
|
|
ADA
|
[NCBI]
|
5.50088e-05
|
|
|
complement component c1r deficiency
|
[NCBI]
|
5.2952e-05
|
|
|
CFD
|
[NCBI]
|
4.53694e-05
|
|
|
FCGR3A
|
[NCBI]
|
4.41286e-05
|
|
|
TNF
|
[NCBI]
|
4.21589e-05
|
|
|
LPO
|
[NCBI]
|
3.8188e-05
|
|
|
complement component 5 deficiency
|
[NCBI]
|
3.81182e-05
|
|
|
IGKC
|
[NCBI]
|
3.75713e-05
|
|
|
C4A
|
[NCBI]
|
3.69913e-05
|
|
|
C4B
|
[NCBI]
|
3.64439e-05
|
|
|
congenital cataracts, facial dysmorphism, and neuropathy
|
[NCBI]
|
3.54021e-05
|
|
|
PI
|
[NCBI]
|
3.50159e-05
|
|
|
SDS
|
[NCBI]
|
3.29467e-05
|
|
|
ERCC2
|
[NCBI]
|
3.29114e-05
|
|
|
XPD
|
[NCBI]
|
3.20816e-05
|
|
|
PHA1
|
[NCBI]
|
3.11238e-05
|
|
|
GSR
|
[NCBI]
|
3.06165e-05
|
|
|
HMGB1
|
[NCBI]
|
2.95155e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.90131e-05
|
|
|
TTDP
|
[NCBI]
|
2.85831e-05
|
|
|
factor x deficiency
|
[NCBI]
|
2.80704e-05
|
|
|
IL4
|
[NCBI]
|
2.52013e-05
|
|
|
RNASE2
|
[NCBI]
|
2.47194e-05
|
|
|
CJD
|
[NCBI]
|
2.43089e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
2.24316e-05
|
|
|
MSS
|
[NCBI]
|
2.14802e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
1.9372e-05
|
|
|
HIGM1
|
[NCBI]
|
1.89899e-05
|
|
|
TLR2
|
[NCBI]
|
1.75906e-05
|
|
|
AT
|
[NCBI]
|
1.70261e-05
|
|
|
OSM
|
[NCBI]
|
1.54615e-05
|
|
|
HNPP
|
[NCBI]
|
1.38819e-05
|
|
|
RTS
|
[NCBI]
|
1.36432e-05
|
|
|
mucolipidosis ii
|
[NCBI]
|
1.36432e-05
|
|
|
sotos syndrome
|
[NCBI]
|
1.36432e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
1.04336e-05
|
|
|
CHH
|
[NCBI]
|
1.04336e-05
|
|
|
IL2
|
[NCBI]
|
1.03901e-05
|
|
|
BLM
|
[NCBI]
|
9.77546e-06
|
|
|
PWS
|
[NCBI]
|
8.20064e-06
|
|
|
CD
|
[NCBI]
|
7.87581e-06
|
|
|
WHS
|
[NCBI]
|
7.67881e-06
|
|
|
MDD
|
[NCBI]
|
4.37983e-06
|
|
|
CEACAM5
|
[NCBI]
|
3.6274e-06
|
|
|
VIP
|
[NCBI]
|
2.03044e-06
|
|
|
BDNF
|
[NCBI]
|
1.18382e-06
|
|
|
PCNA
|
[NCBI]
|
5.38399e-07
|
|
|
AFP
|
[NCBI]
|
1.88133e-07
|
|
|
NGFB
|
[NCBI]
|
1.58102e-07
|
|