MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Extrachromosomal Inheritance
[NCBI]
Gene
Gene
Link
Information
Gain
01
TRNI
[NCBI]
0.000157606
RNR2
[NCBI]
0.000141376
RAG1
[NCBI]
4.24148e-06
DUX4
[NCBI]
3.89584e-06
DHFR
[NCBI]
3.89461e-06
MSTO1
[NCBI]
3.85026e-06
UQCRH
[NCBI]
3.77088e-06
PATZ1
[NCBI]
3.70332e-06
KIF20B
[NCBI]
3.54573e-06
KIN
[NCBI]
3.48358e-06
ATP6
[NCBI]
3.46462e-06
SLIT2
[NCBI]
3.24732e-06
POLI
[NCBI]
3.16342e-06
RPL14
[NCBI]
3.06096e-06
HLA-F
[NCBI]
2.83172e-06
EGFR
[NCBI]
2.8129e-06
PRL
[NCBI]
2.78749e-06
TFAM
[NCBI]
2.75152e-06
HEBP1
[NCBI]
2.7363e-06
CAD
[NCBI]
2.57699e-06
ALB
[NCBI]
2.03802e-06
MLL
[NCBI]
1.9258e-06
HMOX1
[NCBI]
1.89971e-06
GJB2
[NCBI]
1.86675e-06
G6PD
[NCBI]
1.75015e-06
HFE
[NCBI]
1.66498e-06
OMIM
OMIM
Link
Information
gain
01
MAFD1
[NCBI]
0.00137138
myoclonic epilepsy, juvenile, 3
[NCBI]
0.000957753
leber optic atrophy
[NCBI]
0.000411365
chloramphenicol toxicity
[NCBI]
0.000380763
hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial
[NCBI]
0.000170507
retinitis pigmentosa-deafness syndrome
[NCBI]
0.000125454
hemochromatosis, neonatal
[NCBI]
0.000113015
MTND2
[NCBI]
0.000108939
diabetes-deafness syndrome, maternally transmitted
[NCBI]
9.43734e-05
CVS
[NCBI]
8.08523e-05
HOS
[NCBI]
6.95186e-05
MTND3
[NCBI]
6.82687e-05
MTCO1
[NCBI]
6.28066e-05
ABL1
[NCBI]
5.84159e-05
KSS
[NCBI]
5.56019e-05
HD
[NCBI]
5.18084e-05
MTTS2
[NCBI]
4.33758e-05
MTTI
[NCBI]
3.48047e-05
MTND4L
[NCBI]
3.24894e-05
MTTS1
[NCBI]
3.21179e-05
MTCO3
[NCBI]
2.95328e-05
MTRNR1
[NCBI]
2.80936e-05
MTND6
[NCBI]
2.79139e-05
MTND5
[NCBI]
2.79139e-05
MTTK
[NCBI]
2.75701e-05
MTCO2
[NCBI]
2.74054e-05
ABO
[NCBI]
2.69372e-05
MTCYB
[NCBI]
2.6231e-05
factor x deficiency
[NCBI]
2.57213e-05
MTND1
[NCBI]
2.51404e-05
MTND4
[NCBI]
2.42207e-05
RP
[NCBI]
2.4008e-05
DHFR
[NCBI]
2.08535e-05
PRNP
[NCBI]
1.69737e-05
ALB
[NCBI]
1.16261e-05
EGFR
[NCBI]
9.07123e-06
PRL
[NCBI]
7.7358e-06
G6PD
[NCBI]
7.08854e-06
Database Center for Life Science