|
OMIM |
Link |
Information gain |
01 |
|
LPL
|
[NCBI]
|
0.000397339
|
|
|
GIP
|
[NCBI]
|
0.00028338
|
|
|
thyrotoxic periodic paralysis
|
[NCBI]
|
0.000236875
|
|
|
CCK
|
[NCBI]
|
0.000189867
|
|
|
hyperlipoproteinemia, type iv
|
[NCBI]
|
0.000169349
|
|
|
G6PD
|
[NCBI]
|
0.000167164
|
|
|
NPY
|
[NCBI]
|
0.000166745
|
|
|
mullerian aplasia
|
[NCBI]
|
0.000125861
|
|
|
malonyl-coa decarboxylase deficiency
|
[NCBI]
|
0.000107811
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
0.000104009
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
0.000104009
|
|
|
GRTH
|
[NCBI]
|
9.79128e-05
|
|
|
fructose-1,6-bisphosphatase deficiency
|
[NCBI]
|
9.79128e-05
|
|
|
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant
|
[NCBI]
|
8.74291e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
8.32777e-05
|
|
|
galactokinase deficiency
|
[NCBI]
|
8.28944e-05
|
|
|
hyperlipoproteinemia, type i
|
[NCBI]
|
7.91266e-05
|
|
|
galactose epimerase deficiency
|
[NCBI]
|
7.91266e-05
|
|
|
GAL
|
[NCBI]
|
7.89169e-05
|
|
|
CF
|
[NCBI]
|
7.68271e-05
|
|
|
propionic acidemia
|
[NCBI]
|
7.39907e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
7.30923e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
7.22289e-05
|
|
|
CSID
|
[NCBI]
|
7.22289e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
7.22289e-05
|
|
|
FPLD2
|
[NCBI]
|
7.22289e-05
|
|
|
glycogen storage disease vii
|
[NCBI]
|
6.44629e-05
|
|
|
SI
|
[NCBI]
|
6.27706e-05
|
|
|
lactase persistence
|
[NCBI]
|
6.22064e-05
|
|
|
pyruvate decarboxylase deficiency
|
[NCBI]
|
6.11605e-05
|
|
|
RA
|
[NCBI]
|
6.05933e-05
|
|
|
porphyria variegata
|
[NCBI]
|
5.14678e-05
|
|
|
maple syrup urine disease
|
[NCBI]
|
5.14678e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
4.7899e-05
|
|
|
UCP3
|
[NCBI]
|
4.64156e-05
|
|
|
PYY
|
[NCBI]
|
3.94104e-05
|
|
|
APOB
|
[NCBI]
|
2.94781e-05
|
|
|
LCT
|
[NCBI]
|
2.61819e-05
|
|
|
SCD
|
[NCBI]
|
2.5147e-05
|
|
|
fructosuria
|
[NCBI]
|
2.44738e-05
|
|
|
GYS2
|
[NCBI]
|
2.44738e-05
|
|
|
ARMET
|
[NCBI]
|
2.35809e-05
|
|
|
THRSP
|
[NCBI]
|
2.2817e-05
|
|
|
LCAT
|
[NCBI]
|
2.14545e-05
|
|
|
ALPI
|
[NCBI]
|
2.10244e-05
|
|
|
SCARB1
|
[NCBI]
|
1.83137e-05
|
|
|
GALE
|
[NCBI]
|
1.83137e-05
|
|
|
CRC
|
[NCBI]
|
1.76834e-05
|
|
|
USF2
|
[NCBI]
|
1.74774e-05
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
1.65376e-05
|
|
|
FASN
|
[NCBI]
|
1.47417e-05
|
|
|
coproporphyria
|
[NCBI]
|
1.36546e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.35338e-05
|
|
|
USF1
|
[NCBI]
|
1.33005e-05
|
|
|
INS
|
[NCBI]
|
1.2513e-05
|
|
|
TNF
|
[NCBI]
|
1.05482e-05
|
|
|
SHBG
|
[NCBI]
|
1.05101e-05
|
|
|
PTH
|
[NCBI]
|
9.24161e-06
|
|
|
LIPC
|
[NCBI]
|
9.16338e-06
|
|
|
PD
|
[NCBI]
|
9.04769e-06
|
|
|
PIGR
|
[NCBI]
|
8.48782e-06
|
|
|
PC
|
[NCBI]
|
8.28326e-06
|
|
|
PAM
|
[NCBI]
|
7.97425e-06
|
|
|
UCP1
|
[NCBI]
|
7.41446e-06
|
|
|
FRAP1
|
[NCBI]
|
6.45808e-06
|
|
|
EGF
|
[NCBI]
|
6.35821e-06
|
|
|
ACHE
|
[NCBI]
|
5.25706e-06
|
|
|
PRL
|
[NCBI]
|
4.89884e-06
|
|
|
AVP
|
[NCBI]
|
4.61996e-06
|
|
|
IAPP
|
[NCBI]
|
3.7053e-06
|
|
|
PCNA
|
[NCBI]
|
3.56024e-06
|
|
|
CTGF
|
[NCBI]
|
1.70743e-06
|
|
|
TH
|
[NCBI]
|
7.14565e-07
|
|
|
TTR
|
[NCBI]
|
6.90682e-07
|
|
|
POMC
|
[NCBI]
|
5.61533e-07
|
|
|
NPPA
|
[NCBI]
|
3.95571e-07
|
|
|
CRH
|
[NCBI]
|
2.05052e-07
|
|
|
F3
|
[NCBI]
|
1.4911e-07
|
|
|
APOE
|
[NCBI]
|
7.25253e-08
|
|