|
OMIM |
Link |
Information gain |
01 |
|
opticocochleodentate degeneration
|
[NCBI]
|
0.003491
|
|
|
d-bifunctional protein deficiency
|
[NCBI]
|
0.00220241
|
|
|
HSD17B4
|
[NCBI]
|
0.000660751
|
|
|
3-@methylglutaconic aciduria, type i
|
[NCBI]
|
0.000383704
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
0.000234385
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000204635
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
0.000181105
|
|
|
beta-hydroxyisobutyryl coa deacylase, deficiency of
|
[NCBI]
|
0.000150444
|
|
|
3-@methylglutaconic aciduria, type iv
|
[NCBI]
|
0.000150444
|
|
|
3-@methylglutaconic aciduria, type iii
|
[NCBI]
|
0.000120461
|
|
|
AUH
|
[NCBI]
|
0.000114317
|
|
|
peroxisomal acyl-coa oxidase deficiency
|
[NCBI]
|
0.000113393
|
|
|
ALD
|
[NCBI]
|
9.60456e-05
|
|
|
EHHADH
|
[NCBI]
|
9.49594e-05
|
|
|
ECHS1
|
[NCBI]
|
9.49594e-05
|
|
|
HIBCH
|
[NCBI]
|
8.47347e-05
|
|
|
BTHS
|
[NCBI]
|
7.69278e-05
|
|
|
HADHB
|
[NCBI]
|
7.08737e-05
|
|
|
PPARA
|
[NCBI]
|
6.98015e-05
|
|
|
ACADM
|
[NCBI]
|
6.08103e-05
|
|
|
HADHA
|
[NCBI]
|
5.96076e-05
|
|
|
ZS
|
[NCBI]
|
5.5607e-05
|
|
|
ECH1
|
[NCBI]
|
4.74093e-05
|
|
|
ACAA1
|
[NCBI]
|
3.71853e-05
|
|
|
ACOX1
|
[NCBI]
|
2.43277e-05
|
|
|
AMACR
|
[NCBI]
|
2.13051e-05
|
|
|
AHR
|
[NCBI]
|
5.97239e-06
|
|
|
CCK
|
[NCBI]
|
8.31621e-07
|
|