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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ophthalmoplegia, Chronic Progressive External [NCBI]

Gene


 Gene Link Information
Gain		 01
C10orf2 [NCBI] 0.000358533
TFAMP1 [NCBI] 0.000340315
POLG [NCBI] 0.000333078
TRNL2 [NCBI] 0.000302506
TRNI [NCBI] 0.000302506
RNR2 [NCBI] 0.000269008
SLC25A4 [NCBI] 0.000148625
SLC25A6 [NCBI] 7.45684e-05
TFAM [NCBI] 4.17145e-05
POLG2 [NCBI] 2.78595e-05
KIF21A [NCBI] 2.12819e-05
SLC25A28 [NCBI] 1.62965e-05
OPA1 [NCBI] 1.5903e-05
CS [NCBI] 1.51396e-05
POLRMT [NCBI] 1.39161e-05
LARS [NCBI] 1.30177e-05
SLC25A5 [NCBI] 1.24344e-05
TYMP [NCBI] 7.43271e-06
HSPD1 [NCBI] 7.25668e-06
MB [NCBI] 6.21811e-06
DMPK [NCBI] 4.65613e-06



OMIM


 OMIM Link Information
gain		 01
CFEOM3 [NCBI] 0.00111789
POLG [NCBI] 0.000852905
KSS [NCBI] 0.000808447
SLC25A4 [NCBI] 0.000689898
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.000589081
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 [NCBI] 0.000549284
SANDO [NCBI] 0.000440995
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 0.000388442
C10ORF2 [NCBI] 0.000347362
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 [NCBI] 0.000295201
PEOA4 [NCBI] 0.000227206
MTTY [NCBI] 0.000165616
CFEOM2 [NCBI] 9.23698e-05
MTTK [NCBI] 9.06865e-05
POLG2 [NCBI] 8.26658e-05
SLC25A28 [NCBI] 8.26658e-05
minicore myopathy with external ophthalmoplegia [NCBI] 7.6169e-05
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 7.6169e-05
CFEOM1 [NCBI] 6.93382e-05
pearson marrow-pancreas syndrome [NCBI] 6.72541e-05
MTTN [NCBI] 6.36884e-05
MTTL2 [NCBI] 6.03129e-05
humanin [NCBI] 5.58044e-05
ACADS [NCBI] 4.13981e-05
LS [NCBI] 3.97366e-05
OPMD [NCBI] 3.40208e-05
MB [NCBI] 2.53008e-05



Database Center for Life Science