|
OMIM |
Link |
Information gain |
01 |
|
APS2
|
[NCBI]
|
0.00151576
|
|
|
flynn-aird syndrome
|
[NCBI]
|
0.00116675
|
|
|
ketoaciduria with mental deficiency and other features
|
[NCBI]
|
0.000948879
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal recessive
|
[NCBI]
|
0.000813359
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant
|
[NCBI]
|
0.000715905
|
|
|
CNC1
|
[NCBI]
|
0.000486916
|
|
|
holoprosencephaly
|
[NCBI]
|
0.000460266
|
|
|
MAS
|
[NCBI]
|
0.000355319
|
|
|
retinohepatoendocrinologic syndrome
|
[NCBI]
|
0.00033621
|
|
|
donohue syndrome
|
[NCBI]
|
0.000265409
|
|
|
MEN2A
|
[NCBI]
|
0.00025048
|
|
|
APS1
|
[NCBI]
|
0.000237748
|
|
|
follicle-stimulating hormone deficiency, isolated
|
[NCBI]
|
0.000156149
|
|
|
SLE
|
[NCBI]
|
0.000130198
|
|
|
GRTH
|
[NCBI]
|
0.000128683
|
|
|
AHO
|
[NCBI]
|
0.000119324
|
|
|
BFLS
|
[NCBI]
|
0.00011885
|
|
|
RA
|
[NCBI]
|
0.000118535
|
|
|
IPEX
|
[NCBI]
|
0.000117201
|
|
|
weaver syndrome
|
[NCBI]
|
0.000112715
|
|
|
anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis
|
[NCBI]
|
0.000111888
|
|
|
craniosynostosis
|
[NCBI]
|
0.000111888
|
|
|
MEN2B
|
[NCBI]
|
0.000102148
|
|
|
KSS
|
[NCBI]
|
9.92271e-05
|
|
|
PRL
|
[NCBI]
|
9.84428e-05
|
|
|
HHC1
|
[NCBI]
|
9.42548e-05
|
|
|
CD
|
[NCBI]
|
9.36724e-05
|
|
|
INSR
|
[NCBI]
|
9.23183e-05
|
|
|
AIS
|
[NCBI]
|
9.21962e-05
|
|
|
CHGA
|
[NCBI]
|
8.70059e-05
|
|
|
CPE
|
[NCBI]
|
7.79722e-05
|
|
|
GPR1
|
[NCBI]
|
7.57054e-05
|
|
|
satoyoshi syndrome
|
[NCBI]
|
7.5473e-05
|
|
|
FOXP3
|
[NCBI]
|
6.8712e-05
|
|
|
orthostatic intolerance
|
[NCBI]
|
6.81454e-05
|
|
|
TTDN1
|
[NCBI]
|
6.54472e-05
|
|
|
POMC
|
[NCBI]
|
5.96548e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
5.49323e-05
|
|
|
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant
|
[NCBI]
|
5.37003e-05
|
|
|
GNAI2
|
[NCBI]
|
5.33599e-05
|
|
|
myxoma, intracardiac
|
[NCBI]
|
5.25576e-05
|
|
|
TTDN1
|
[NCBI]
|
4.88563e-05
|
|
|
alexander disease
|
[NCBI]
|
4.78347e-05
|
|
|
PCSK1
|
[NCBI]
|
4.57765e-05
|
|
|
acromegaly
|
[NCBI]
|
4.48743e-05
|
|
|
FSTL3
|
[NCBI]
|
4.45356e-05
|
|
|
FSHB
|
[NCBI]
|
4.45356e-05
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
4.42149e-05
|
|
|
MADA
|
[NCBI]
|
4.35826e-05
|
|
|
RBP3
|
[NCBI]
|
4.34336e-05
|
|
|
POF1
|
[NCBI]
|
4.29751e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
4.1828e-05
|
|
|
CGL2
|
[NCBI]
|
4.1828e-05
|
|
|
PTH
|
[NCBI]
|
4.16562e-05
|
|
|
HFE
|
[NCBI]
|
4.05082e-05
|
|
|
SLC16A2
|
[NCBI]
|
3.99576e-05
|
|
|
graves disease
|
[NCBI]
|
3.92886e-05
|
|
|
GHRH
|
[NCBI]
|
3.90979e-05
|
|
|
OCA2
|
[NCBI]
|
3.71145e-05
|
|
|
CRH
|
[NCBI]
|
3.64997e-05
|
|
|
PRKAR1A
|
[NCBI]
|
3.63302e-05
|
|
|
CF
|
[NCBI]
|
3.58684e-05
|
|
|
APTX
|
[NCBI]
|
3.4922e-05
|
|
|
CSA
|
[NCBI]
|
3.23136e-05
|
|
|
BRRS
|
[NCBI]
|
3.03982e-05
|
|
|
AVP
|
[NCBI]
|
3.03529e-05
|
|
|
AR
|
[NCBI]
|
2.95364e-05
|
|
|
TF
|
[NCBI]
|
2.93142e-05
|
|
|
THRB
|
[NCBI]
|
2.76151e-05
|
|
|
GH1
|
[NCBI]
|
2.61067e-05
|
|
|
PNMT
|
[NCBI]
|
2.36664e-05
|
|
|
GNAS
|
[NCBI]
|
2.24137e-05
|
|
|
AIRE
|
[NCBI]
|
2.21825e-05
|
|
|
SHBG
|
[NCBI]
|
2.05659e-05
|
|
|
CD
|
[NCBI]
|
2.04314e-05
|
|
|
CDLS1
|
[NCBI]
|
2.04314e-05
|
|
|
GAL
|
[NCBI]
|
1.93602e-05
|
|
|
VHL
|
[NCBI]
|
1.9037e-05
|
|
|
MEN1
|
[NCBI]
|
1.87163e-05
|
|
|
CASR
|
[NCBI]
|
1.8639e-05
|
|
|
MDD
|
[NCBI]
|
1.80947e-05
|
|
|
SMAX1
|
[NCBI]
|
1.7299e-05
|
|
|
AMH
|
[NCBI]
|
1.69639e-05
|
|
|
IAPP
|
[NCBI]
|
1.54033e-05
|
|
|
BCNS
|
[NCBI]
|
1.51349e-05
|
|
|
PJS
|
[NCBI]
|
1.18363e-05
|
|
|
AT
|
[NCBI]
|
7.04079e-06
|
|
|
VEGF
|
[NCBI]
|
5.40161e-06
|
|
|
KLK3
|
[NCBI]
|
3.28239e-06
|
|
|
CEACAM5
|
[NCBI]
|
3.19002e-06
|
|
|
FA
|
[NCBI]
|
1.99928e-06
|
|
|
TG
|
[NCBI]
|
1.75144e-06
|
|
|
FMF
|
[NCBI]
|
1.44848e-06
|
|
|
MG
|
[NCBI]
|
8.97955e-07
|
|
|
TH
|
[NCBI]
|
8.92879e-07
|
|
|
NPY
|
[NCBI]
|
3.03992e-07
|
|
|
EPO
|
[NCBI]
|
6.86656e-08
|
|