|
OMIM |
Link |
Information gain |
01 |
|
mitochondrial complex iii deficiency
|
[NCBI]
|
0.00048327
|
|
|
CGD
|
[NCBI]
|
0.000297103
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
|
[NCBI]
|
0.000219576
|
|
|
hypermetabolism due to defect in mitochondria
|
[NCBI]
|
0.000191006
|
|
|
MLASA
|
[NCBI]
|
0.00013401
|
|
|
gracile syndrome
|
[NCBI]
|
0.000116971
|
|
|
CYP1A1
|
[NCBI]
|
0.000114207
|
|
|
sulfocysteinuria
|
[NCBI]
|
0.000110728
|
|
|
hypoascorbemia
|
[NCBI]
|
0.000108978
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
0.000105839
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
8.70523e-05
|
|
|
MTCYB
|
[NCBI]
|
8.69786e-05
|
|
|
BTHS
|
[NCBI]
|
8.58133e-05
|
|
|
ZS
|
[NCBI]
|
6.43411e-05
|
|
|
CYP2A6
|
[NCBI]
|
5.49194e-05
|
|
|
MB
|
[NCBI]
|
4.68416e-05
|
|
|
MTTL2
|
[NCBI]
|
3.64407e-05
|
|
|
PUS1
|
[NCBI]
|
3.50883e-05
|
|
|
BCS1L
|
[NCBI]
|
3.23476e-05
|
|
|
CYP2E
|
[NCBI]
|
2.96127e-05
|
|
|
ATP5O
|
[NCBI]
|
2.88188e-05
|
|
|
TAZ
|
[NCBI]
|
2.81278e-05
|
|
|
prekallikrein deficiency
|
[NCBI]
|
2.78133e-05
|
|
|
MTCO3
|
[NCBI]
|
2.55964e-05
|
|
|
SLC25A4
|
[NCBI]
|
2.4846e-05
|
|
|
MTTK
|
[NCBI]
|
2.41885e-05
|
|
|
MTCO1
|
[NCBI]
|
2.36035e-05
|
|
|
FXN
|
[NCBI]
|
2.19512e-05
|
|
|
SOD1
|
[NCBI]
|
1.29904e-05
|
|
|
TG
|
[NCBI]
|
5.20602e-06
|
|
|
CAT
|
[NCBI]
|
3.20284e-06
|
|
|
MPO
|
[NCBI]
|
2.10418e-06
|
|
|
ACHE
|
[NCBI]
|
9.12403e-07
|
|
|
EGFR
|
[NCBI]
|
8.35112e-07
|
|
|
NGFB
|
[NCBI]
|
2.03809e-07
|
|