|
OMIM |
Link |
Information gain |
01 |
|
methylmalonic aciduria and homocystinuria, cbld type
|
[NCBI]
|
0.00501703
|
|
|
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
|
[NCBI]
|
0.00291478
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
0.00198548
|
|
|
methylmalonic aciduria, cbla type
|
[NCBI]
|
0.00101559
|
|
|
MUT
|
[NCBI]
|
0.000531065
|
|
|
methylmalonic aciduria, cblb type
|
[NCBI]
|
0.000491896
|
|
|
pancreatic beta cell agenesis with neonatal diabetes mellitus
|
[NCBI]
|
0.000327449
|
|
|
methylmalonyl-coa epimerase deficiency
|
[NCBI]
|
0.000283951
|
|
|
methylmalonic aciduria, cblh type
|
[NCBI]
|
0.000131914
|
|
|
malonyl-coa decarboxylase deficiency
|
[NCBI]
|
0.000101969
|
|
|
RA
|
[NCBI]
|
9.77464e-05
|
|
|
MMAA
|
[NCBI]
|
9.61509e-05
|
|
|
SLE
|
[NCBI]
|
9.08333e-05
|
|
|
methylcobalamin deficiency, cblg type
|
[NCBI]
|
8.95626e-05
|
|
|
MCEE
|
[NCBI]
|
8.59261e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
8.4403e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
8.16187e-05
|
|
|
hartnup disorder
|
[NCBI]
|
8.00069e-05
|
|
|
mmachc gene
|
[NCBI]
|
4.79967e-05
|
|
|
MTR
|
[NCBI]
|
4.50919e-05
|
|
|
MMAB
|
[NCBI]
|
4.05739e-05
|
|
|
SUCLA2
|
[NCBI]
|
3.77726e-05
|
|
|
MLYCD
|
[NCBI]
|
3.05948e-05
|
|
|
CUBN
|
[NCBI]
|
2.59844e-05
|
|
|
SPR
|
[NCBI]
|
2.57522e-05
|
|
|
MTHFR
|
[NCBI]
|
1.88777e-05
|
|
|
ACADM
|
[NCBI]
|
1.4883e-05
|
|
|
ALB
|
[NCBI]
|
8.43164e-06
|
|
|
CAT
|
[NCBI]
|
2.84986e-06
|
|
|
GFAP
|
[NCBI]
|
1.29026e-06
|
|
|
EPO
|
[NCBI]
|
1.2853e-06
|
|
|
PCNA
|
[NCBI]
|
1.12104e-06
|
|
|
PTH
|
[NCBI]
|
1.79249e-07
|
|