|
OMIM |
Link |
Information gain |
01 |
|
APS2
|
[NCBI]
|
0.00265676
|
|
|
thyroid hormonogenesis, genetic defect in, 4
|
[NCBI]
|
0.00222651
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.00210699
|
|
|
TG
|
[NCBI]
|
0.00179734
|
|
|
CHNG2
|
[NCBI]
|
0.00155276
|
|
|
TPO
|
[NCBI]
|
0.00118761
|
|
|
megalocornea-mental retardation syndrome
|
[NCBI]
|
0.00109496
|
|
|
PRL
|
[NCBI]
|
0.000900531
|
|
|
thyroid hormonogenesis, genetic defect in, 2a
|
[NCBI]
|
0.000823054
|
|
|
CHNG1
|
[NCBI]
|
0.000764676
|
|
|
thyrotropin deficiency, isolated
|
[NCBI]
|
0.00071337
|
|
|
CHNG3
|
[NCBI]
|
0.000652698
|
|
|
MCOPS6
|
[NCBI]
|
0.000503004
|
|
|
hennekam lymphangiectasia-lymphedema syndrome
|
[NCBI]
|
0.000480827
|
|
|
SLC5A5
|
[NCBI]
|
0.000468052
|
|
|
AHO
|
[NCBI]
|
0.000454062
|
|
|
TSHB
|
[NCBI]
|
0.000382492
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
0.000377087
|
|
|
IGAD1
|
[NCBI]
|
0.000320195
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.000263751
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000254795
|
|
|
choreoathetosis, hypothyroidism, and neonatal respiratory distress
|
[NCBI]
|
0.000245703
|
|
|
young-simpson syndrome
|
[NCBI]
|
0.000235654
|
|
|
FOXE1
|
[NCBI]
|
0.000217525
|
|
|
RA
|
[NCBI]
|
0.000212868
|
|
|
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia
|
[NCBI]
|
0.000208582
|
|
|
TSHR
|
[NCBI]
|
0.000188937
|
|
|
VEGF
|
[NCBI]
|
0.000178141
|
|
|
thyroid hormonogenesis, genetic defect in, 6
|
[NCBI]
|
0.000177653
|
|
|
SHBG
|
[NCBI]
|
0.000155996
|
|
|
thyroid hormonogenesis, genetic defect in, 1
|
[NCBI]
|
0.00015411
|
|
|
PAX8
|
[NCBI]
|
0.000142847
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
0.000140823
|
|
|
CTNS
|
[NCBI]
|
0.000126536
|
|
|
CMH
|
[NCBI]
|
0.000121549
|
|
|
thyrotropin-releasing hormone deficiency
|
[NCBI]
|
0.000114444
|
|
|
BWS
|
[NCBI]
|
0.000113961
|
|
|
TNF
|
[NCBI]
|
0.00011223
|
|
|
pituitary dwarfism with large sella turcica
|
[NCBI]
|
0.000104234
|
|
|
JBS
|
[NCBI]
|
9.75569e-05
|
|
|
NKX2-1
|
[NCBI]
|
9.74593e-05
|
|
|
POU1F1
|
[NCBI]
|
9.15485e-05
|
|
|
graves disease
|
[NCBI]
|
8.61061e-05
|
|
|
CF
|
[NCBI]
|
8.54656e-05
|
|
|
PAM
|
[NCBI]
|
8.37947e-05
|
|
|
BGLAP
|
[NCBI]
|
8.20901e-05
|
|
|
LPL
|
[NCBI]
|
8.18332e-05
|
|
|
chondrocalcinosis due to apatite crystal deposition
|
[NCBI]
|
8.17879e-05
|
|
|
ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum
|
[NCBI]
|
8.17879e-05
|
|
|
VIP
|
[NCBI]
|
7.68854e-05
|
|
|
EGFR
|
[NCBI]
|
7.36915e-05
|
|
|
dicarboxylicamino aciduria
|
[NCBI]
|
7.33318e-05
|
|
|
PDS
|
[NCBI]
|
7.06802e-05
|
|
|
SLC26A4
|
[NCBI]
|
6.84656e-05
|
|
|
DUOX2
|
[NCBI]
|
6.7273e-05
|
|
|
AVP
|
[NCBI]
|
6.61631e-05
|
|
|
IDDM12
|
[NCBI]
|
6.37796e-05
|
|
|
thyroglossal duct cyst, familial
|
[NCBI]
|
6.37796e-05
|
|
|
LIPC
|
[NCBI]
|
5.81227e-05
|
|
|
DIO3
|
[NCBI]
|
5.72112e-05
|
|
|
TOMM70A
|
[NCBI]
|
5.72112e-05
|
|
|
MIRN208
|
[NCBI]
|
5.72112e-05
|
|
|
AITD3
|
[NCBI]
|
5.55556e-05
|
|
|
atransferrinemia
|
[NCBI]
|
5.355e-05
|
|
|
osseous heteroplasia, progressive
|
[NCBI]
|
5.355e-05
|
|
|
APS1
|
[NCBI]
|
5.10125e-05
|
|
|
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
|
[NCBI]
|
5.01735e-05
|
|
|
crigler-najjar syndrome, type ii
|
[NCBI]
|
4.87238e-05
|
|
|
lipomatosis, familial benign cervical
|
[NCBI]
|
4.87238e-05
|
|
|
myotonia congenita, autosomal recessive
|
[NCBI]
|
4.87238e-05
|
|
|
17-@beta hydroxysteroid dehydrogenase iii deficiency
|
[NCBI]
|
4.50425e-05
|
|
|
pituitary dwarfism iii
|
[NCBI]
|
4.39871e-05
|
|
|
TECTB
|
[NCBI]
|
4.34619e-05
|
|
|
SRG1
|
[NCBI]
|
4.34619e-05
|
|
|
EEC3
|
[NCBI]
|
4.29993e-05
|
|
|
EPO
|
[NCBI]
|
4.21941e-05
|
|
|
hyperlipoproteinemia, type i
|
[NCBI]
|
4.20713e-05
|
|
|
AHDS
|
[NCBI]
|
4.20713e-05
|
|
|
pseudohypoparathyroidism, type ib
|
[NCBI]
|
4.20713e-05
|
|
|
JBS
|
[NCBI]
|
4.11963e-05
|
|
|
SERPINA6
|
[NCBI]
|
3.99966e-05
|
|
|
myotonia congenita, autosomal dominant
|
[NCBI]
|
3.9584e-05
|
|
|
gilbert syndrome
|
[NCBI]
|
3.88379e-05
|
|
|
DUOX1
|
[NCBI]
|
3.8292e-05
|
|
|
weaver syndrome
|
[NCBI]
|
3.74479e-05
|
|
|
ALMS
|
[NCBI]
|
3.55782e-05
|
|
|
MB
|
[NCBI]
|
3.54753e-05
|
|
|
PVALB
|
[NCBI]
|
3.49456e-05
|
|
|
SIX6
|
[NCBI]
|
3.49456e-05
|
|
|
SLE
|
[NCBI]
|
3.30011e-05
|
|
|
DIO2
|
[NCBI]
|
3.24654e-05
|
|
|
ACHE
|
[NCBI]
|
3.08003e-05
|
|
|
TBS
|
[NCBI]
|
3.06484e-05
|
|
|
APOB
|
[NCBI]
|
3.06232e-05
|
|
|
PXE
|
[NCBI]
|
2.83755e-05
|
|
|
MYH6
|
[NCBI]
|
2.74687e-05
|
|
|
down syndrome
|
[NCBI]
|
2.63533e-05
|
|
|
MPO
|
[NCBI]
|
2.63355e-05
|
|
|
GNPAT
|
[NCBI]
|
2.62544e-05
|
|
|
CHAT
|
[NCBI]
|
2.60009e-05
|
|
|
UCP1
|
[NCBI]
|
2.57958e-05
|
|
|
RTN1
|
[NCBI]
|
2.51791e-05
|
|
|
CSF1R
|
[NCBI]
|
2.51791e-05
|
|
|
AD
|
[NCBI]
|
2.49534e-05
|
|
|
HAE
|
[NCBI]
|
2.33265e-05
|
|
|
MAG
|
[NCBI]
|
2.24526e-05
|
|
|
SLC16A2
|
[NCBI]
|
2.18096e-05
|
|
|
ATF6
|
[NCBI]
|
2.11304e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
2.06612e-05
|
|
|
PON1
|
[NCBI]
|
1.97317e-05
|
|
|
APOE
|
[NCBI]
|
1.94064e-05
|
|
|
GNMT
|
[NCBI]
|
1.93549e-05
|
|
|
TTR
|
[NCBI]
|
1.84433e-05
|
|
|
PROP1
|
[NCBI]
|
1.83419e-05
|
|
|
GAL
|
[NCBI]
|
1.80222e-05
|
|
|
AFP
|
[NCBI]
|
1.70352e-05
|
|
|
GHR
|
[NCBI]
|
1.67685e-05
|
|
|
OMP
|
[NCBI]
|
1.66127e-05
|
|
|
CEACAM5
|
[NCBI]
|
1.63635e-05
|
|
|
TP73L
|
[NCBI]
|
1.62299e-05
|
|
|
AR
|
[NCBI]
|
1.60767e-05
|
|
|
TH
|
[NCBI]
|
1.50012e-05
|
|
|
CST3
|
[NCBI]
|
1.48524e-05
|
|
|
CTLA4
|
[NCBI]
|
1.48524e-05
|
|
|
PCNA
|
[NCBI]
|
1.42651e-05
|
|
|
CCK
|
[NCBI]
|
1.21492e-05
|
|
|
UCP3
|
[NCBI]
|
1.15259e-05
|
|
|
GNRH1
|
[NCBI]
|
1.15177e-05
|
|
|
NPY
|
[NCBI]
|
1.13979e-05
|
|
|
F3
|
[NCBI]
|
1.05457e-05
|
|
|
KSS
|
[NCBI]
|
1.04963e-05
|
|
|
THRB
|
[NCBI]
|
1.03725e-05
|
|
|
AQP2
|
[NCBI]
|
1.01969e-05
|
|
|
G6PD
|
[NCBI]
|
1.01743e-05
|
|
|
MG
|
[NCBI]
|
9.71375e-06
|
|
|
MYH7
|
[NCBI]
|
9.69476e-06
|
|
|
STAT5A
|
[NCBI]
|
8.64834e-06
|
|
|
OXT
|
[NCBI]
|
8.51135e-06
|
|
|
MDD
|
[NCBI]
|
8.18332e-06
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
7.89639e-06
|
|
|
GHRH
|
[NCBI]
|
7.8798e-06
|
|
|
FA
|
[NCBI]
|
7.49387e-06
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
7.39463e-06
|
|
|
LCAT
|
[NCBI]
|
7.31852e-06
|
|
|
ADA
|
[NCBI]
|
6.28841e-06
|
|
|
IGFALS
|
[NCBI]
|
6.26076e-06
|
|
|
GIP
|
[NCBI]
|
5.88956e-06
|
|
|
VDR
|
[NCBI]
|
5.80788e-06
|
|
|
ACADM
|
[NCBI]
|
5.47822e-06
|
|
|
PWS
|
[NCBI]
|
4.80215e-06
|
|
|
MBP
|
[NCBI]
|
3.54394e-06
|
|
|
MAP2
|
[NCBI]
|
3.17183e-06
|
|
|
LEP
|
[NCBI]
|
2.98601e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
2.97163e-06
|
|
|
GFAP
|
[NCBI]
|
2.883e-06
|
|
|
SPP1
|
[NCBI]
|
2.81863e-06
|
|
|
NPPA
|
[NCBI]
|
2.40789e-06
|
|
|
PDCD8
|
[NCBI]
|
2.40681e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
2.39983e-06
|
|
|
CVID
|
[NCBI]
|
2.34698e-06
|
|
|
SOD2
|
[NCBI]
|
2.25278e-06
|
|
|
TF
|
[NCBI]
|
2.23148e-06
|
|
|
NGFB
|
[NCBI]
|
1.21876e-06
|
|
|
PTH
|
[NCBI]
|
6.37302e-07
|
|
|
temporal arteritis
|
[NCBI]
|
6.02591e-07
|
|
|
BDNF
|
[NCBI]
|
5.60638e-07
|
|
|
CP
|
[NCBI]
|
5.11801e-07
|
|
|
CRH
|
[NCBI]
|
3.90473e-07
|
|
|
TFPI
|
[NCBI]
|
3.11818e-07
|
|
|
CAT
|
[NCBI]
|
1.71561e-07
|
|
|
ALB
|
[NCBI]
|
1.53152e-07
|
|
|
COMT
|
[NCBI]
|
1.43384e-07
|
|
|
EGF
|
[NCBI]
|
1.12259e-07
|
|
|
RP
|
[NCBI]
|
7.9532e-08
|
|
|
CD
|
[NCBI]
|
5.89457e-08
|
|
|
GAPDH
|
[NCBI]
|
8.89641e-09
|
|