|
OMIM |
Link |
Information gain |
01 |
|
EKD1
|
[NCBI]
|
0.0011991
|
|
|
pulmonary alveolar proteinosis, acquired
|
[NCBI]
|
0.000801832
|
|
|
VUR1
|
[NCBI]
|
0.000593468
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000593468
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.000543053
|
|
|
PPR
|
[NCBI]
|
0.000481279
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000426468
|
|
|
GACI
|
[NCBI]
|
0.000143559
|
|
|
fertile eunuch syndrome
|
[NCBI]
|
0.000133162
|
|
|
aniridia, microcornea, and spontaneously reabsorbed cataract
|
[NCBI]
|
0.000133162
|
|
|
ankyloblepharon filiforme adnatum and cleft palate
|
[NCBI]
|
0.000105414
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
9.65364e-05
|
|
|
CEACAM5
|
[NCBI]
|
9.41371e-05
|
|
|
FHL4
|
[NCBI]
|
8.81752e-05
|
|
|
seizures, benign familial neonatal-infantile
|
[NCBI]
|
8.31389e-05
|
|
|
ectodermal dysplasia, hypohidrotic, with immune deficiency
|
[NCBI]
|
7.91307e-05
|
|
|
PDV
|
[NCBI]
|
7.58018e-05
|
|
|
citrullinemia, type ii, neonatal-onset
|
[NCBI]
|
7.29558e-05
|
|
|
GGM
|
[NCBI]
|
7.04708e-05
|
|
|
GTS
|
[NCBI]
|
6.90196e-05
|
|
|
CTLN2
|
[NCBI]
|
6.8266e-05
|
|
|
osteoporosis, juvenile
|
[NCBI]
|
6.44872e-05
|
|
|
RA
|
[NCBI]
|
6.23207e-05
|
|
|
BHC
|
[NCBI]
|
5.99184e-05
|
|
|
propionic acidemia
|
[NCBI]
|
5.99184e-05
|
|
|
alexander disease
|
[NCBI]
|
5.86077e-05
|
|
|
CF
|
[NCBI]
|
5.83608e-05
|
|
|
NPHS1
|
[NCBI]
|
5.73806e-05
|
|
|
MBP
|
[NCBI]
|
5.71123e-05
|
|
|
GABEB
|
[NCBI]
|
5.62273e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
5.22058e-05
|
|
|
SEDC
|
[NCBI]
|
4.96662e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
4.96662e-05
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
3.90958e-05
|
|
|
STX11
|
[NCBI]
|
3.37934e-05
|
|
|
MG
|
[NCBI]
|
3.3719e-05
|
|
|
temporal arteritis
|
[NCBI]
|
3.21092e-05
|
|
|
IL12RB2
|
[NCBI]
|
3.1947e-05
|
|
|
SLC25A13
|
[NCBI]
|
3.1947e-05
|
|
|
MAF
|
[NCBI]
|
3.12028e-05
|
|
|
MIRN16-1
|
[NCBI]
|
3.12028e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
3.07479e-05
|
|
|
PSORS1
|
[NCBI]
|
2.84381e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
2.77352e-05
|
|
|
ITGB4
|
[NCBI]
|
2.65867e-05
|
|
|
LAMB3
|
[NCBI]
|
2.51699e-05
|
|
|
DBA
|
[NCBI]
|
2.40657e-05
|
|
|
IL12B
|
[NCBI]
|
2.30738e-05
|
|
|
IKBKG
|
[NCBI]
|
2.27315e-05
|
|
|
PIGA
|
[NCBI]
|
2.25676e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
2.19542e-05
|
|
|
GNRHR
|
[NCBI]
|
1.97907e-05
|
|
|
DNTT
|
[NCBI]
|
1.91277e-05
|
|
|
RNASE3
|
[NCBI]
|
1.83044e-05
|
|
|
AFP
|
[NCBI]
|
1.68135e-05
|
|
|
GJB1
|
[NCBI]
|
1.54329e-05
|
|
|
ADA
|
[NCBI]
|
1.53931e-05
|
|
|
PTH
|
[NCBI]
|
1.45099e-05
|
|
|
SLE
|
[NCBI]
|
1.3459e-05
|
|
|
ALK
|
[NCBI]
|
1.24593e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.19629e-05
|
|
|
AVP
|
[NCBI]
|
1.08641e-05
|
|
|
MDD
|
[NCBI]
|
9.47558e-06
|
|
|
HGF
|
[NCBI]
|
7.11487e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
6.87869e-06
|
|
|
SLC6A3
|
[NCBI]
|
5.45391e-06
|
|
|
VEGF
|
[NCBI]
|
4.07835e-06
|
|
|
FMF
|
[NCBI]
|
2.2172e-06
|
|
|
LPL
|
[NCBI]
|
1.41506e-06
|
|
|
CD
|
[NCBI]
|
9.87447e-07
|
|
|
MPO
|
[NCBI]
|
9.08579e-07
|
|
|
VIP
|
[NCBI]
|
5.27042e-07
|
|
|
TH
|
[NCBI]
|
1.41352e-07
|
|
|
PRL
|
[NCBI]
|
5.03076e-08
|
|
|
TNF
|
[NCBI]
|
2.80443e-08
|
|