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MeSH keywords -> Related genes, diseases (OMIM)


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01 Optic Atrophy, Autosomal Dominant [NCBI]

Gene


 Gene Link Information
Gain		 01
OPA1 [NCBI] 0.000972383
OPA5 [NCBI] 0.000938495
OPA4 [NCBI] 0.000378131
OPA3 [NCBI] 3.6084e-05
MFN2 [NCBI] 7.95587e-06
OPTN [NCBI] 7.28074e-06



OMIM


 OMIM Link Information
gain		 01
OPA5 [NCBI] 0.00159179
OPA1 [NCBI] 0.00120024
OPA4 [NCBI] 0.00119841
OPA1 [NCBI] 0.000847573
optic atrophy 1 and deafness [NCBI] 0.000506354
optic atrophy 3, autosomal dominant [NCBI] 0.000112852
leber optic atrophy [NCBI] 0.000110128
hereditary motor and sensory neuropathy vi [NCBI] 0.000103252
DFNA6 [NCBI] 8.80291e-05
NCAPG [NCBI] 8.00936e-05
OPA3 [NCBI] 7.48929e-05
SDHA [NCBI] 6.7004e-05
WFS1 [NCBI] 6.58032e-05
TIMM8A [NCBI] 6.05698e-05
WFS1 [NCBI] 5.29997e-05



Database Center for Life Science