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MeSH keywords -> Related genes, diseases (OMIM)


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01 Bulbar Palsy, Progressive [NCBI]

Gene


 Gene Link Information
Gain		 01
AR [NCBI] 3.02754e-05
NAIP [NCBI] 9.82166e-06
MUSK [NCBI] 9.69712e-06
SPAST [NCBI] 9.60615e-06
TTR [NCBI] 7.27215e-06
CCK [NCBI] 6.05798e-06
SOD1 [NCBI] 5.99767e-06
CASP3 [NCBI] 4.2708e-06



OMIM


 OMIM Link Information
gain		 01
bulbar palsy, progressive, with sensorineural deafness [NCBI] 0.00307428
bulbar palsy, progressive, of childhood [NCBI] 0.00236515
SMAX1 [NCBI] 0.000491068
MBS [NCBI] 0.000464945
spinal muscular atrophy, proximal, adult, autosomal dominant [NCBI] 0.000214516
whispering dysphonia, hereditary [NCBI] 0.000145155
AR [NCBI] 0.000127557
spinal muscular atrophy, scapuloperoneal [NCBI] 0.000122684
suprabulbar paresis, congenital [NCBI] 0.000122684
SMA4 [NCBI] 9.08533e-05
PLSJ [NCBI] 9.08533e-05
alsin [NCBI] 6.3036e-05
NPC1 [NCBI] 5.92121e-05
TTR [NCBI] 2.65885e-05
FTD [NCBI] 2.629e-05
CCK [NCBI] 2.05491e-05



Database Center for Life Science