|
OMIM |
Link |
Information
gain |
01 |
|
|
hydroxykynureninuria
|
[NCBI]
|
0.00119841
|
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
0.000379458
|
|
|
|
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
|
[NCBI]
|
0.000261675
|
|
|
|
FHM2
|
[NCBI]
|
0.000258811
|
|
|
|
IVA
|
[NCBI]
|
0.000146007
|
|
|
|
3-@hydroxy-3-methylglutaryl-coa synthase 2, mitochondrial, deficiency of
|
[NCBI]
|
0.000107971
|
|
|
|
CACNA1A
|
[NCBI]
|
8.77963e-05
|
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
8.39316e-05
|
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
8.16129e-05
|
|
|
|
colloid cysts of third ventricle
|
[NCBI]
|
7.95864e-05
|
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
6.7023e-05
|
|
|
|
AVP
|
[NCBI]
|
6.4475e-05
|
|
|
|
HMGCS2
|
[NCBI]
|
6.28498e-05
|
|
|
|
GCE
|
[NCBI]
|
6.06417e-05
|
|
|
|
hyperglycerolemia
|
[NCBI]
|
6.06417e-05
|
|
|
|
AHC
|
[NCBI]
|
5.84605e-05
|
|
|
|
FHM1
|
[NCBI]
|
5.84605e-05
|
|
|
|
CDSP
|
[NCBI]
|
5.74727e-05
|
|
|
|
malaria, susceptibility to
|
[NCBI]
|
5.65428e-05
|
|
|
|
ASL
|
[NCBI]
|
5.01809e-05
|
|
|
|
CTNS
|
[NCBI]
|
4.99856e-05
|
|
|
|
ATP1A2
|
[NCBI]
|
4.94173e-05
|
|
|
|
PRL
|
[NCBI]
|
4.86771e-05
|
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
4.52764e-05
|
|
|
|
TNFRSF1B
|
[NCBI]
|
4.43546e-05
|
|
|
|
LPI
|
[NCBI]
|
4.43059e-05
|
|
|
|
SLC4A1
|
[NCBI]
|
3.4922e-05
|
|
|
|
ABCD1
|
[NCBI]
|
3.39625e-05
|
|
|
|
ACADM
|
[NCBI]
|
3.08622e-05
|
|
|
|
CP
|
[NCBI]
|
2.18605e-05
|
|
|
|
ALD
|
[NCBI]
|
1.82741e-05
|
|
|
|
ADA
|
[NCBI]
|
1.01761e-05
|
|
|
|
TNF
|
[NCBI]
|
8.3322e-06
|
|
|
|
BDNF
|
[NCBI]
|
7.40556e-06
|
|
|
|
TH
|
[NCBI]
|
6.5157e-06
|
|
|
|
CJD
|
[NCBI]
|
6.30464e-06
|
|
|
|
MBP
|
[NCBI]
|
4.98367e-06
|
|
|
|
GFAP
|
[NCBI]
|
2.93313e-06
|
|
|
|
AFP
|
[NCBI]
|
2.52462e-06
|
|
|
|
SLE
|
[NCBI]
|
6.54719e-07
|
|
|
|
PTH
|
[NCBI]
|
4.09112e-07
|
|
