Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Muscle Hypertonia	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000117314
GLRA1	[NCBI]	5.56696e-05
GER	[NCBI]	5.38017e-05
TRAK1	[NCBI]	3.40503e-05
TRAK2	[NCBI]	1.5332e-05
GCHFR	[NCBI]	1.43147e-05
SLC6A5	[NCBI]	1.3969e-05
ALG12	[NCBI]	1.36815e-05
NSF	[NCBI]	1.27007e-05
KCNMA1	[NCBI]	1.14735e-05
HGS	[NCBI]	1.1402e-05
SCN4A	[NCBI]	9.08612e-06
PTGER1	[NCBI]	8.9302e-06
MSTN	[NCBI]	8.75712e-06
TRPV1	[NCBI]	8.59996e-06
PMP22	[NCBI]	6.54143e-06
NGF	[NCBI]	3.67239e-06

OMIM	Link	Information gain
microcephaly, hiatus hernia, and nephrotic syndrome	[NCBI]	0.000880362
hyperekplexia, hereditary	[NCBI]	0.000672013
SPS	[NCBI]	0.000603963
GLRA1	[NCBI]	0.000291873
yemenite deaf-blind hypopigmentation syndrome	[NCBI]	0.000112852
CDG1G	[NCBI]	0.000107346
stuve-wiedemann syndrome	[NCBI]	8.42761e-05
TRAK1	[NCBI]	8.00936e-05
weaver syndrome	[NCBI]	7.64665e-05
infantile sialic acid storage disorder	[NCBI]	7.45252e-05
ALG12	[NCBI]	7.15158e-05
COH1	[NCBI]	6.69024e-05
SLC1A3	[NCBI]	6.26709e-05
NSF	[NCBI]	6.15648e-05
SOX10	[NCBI]	5.21546e-05
DPYD	[NCBI]	4.93514e-05
tyrosinemia, type i	[NCBI]	4.22596e-05
NGFB	[NCBI]	8.74059e-06
AD	[NCBI]	6.80853e-06