Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Vocal Cords	[NCBI]

Gene	Link	Information Gain
HMN7A	[NCBI]	0.000466155
MPD2	[NCBI]	0.000466155
GER	[NCBI]	0.000102676
HGF	[NCBI]	2.92263e-05
EGFR	[NCBI]	8.58992e-06
EN1	[NCBI]	6.39446e-06
MYOT	[NCBI]	6.3061e-06
ASAH1	[NCBI]	5.89573e-06
HAS2	[NCBI]	5.51226e-06
PCNA	[NCBI]	5.40101e-06
KRT5	[NCBI]	5.31629e-06
TFF3	[NCBI]	5.26528e-06
TGM1	[NCBI]	4.85526e-06
KRT14	[NCBI]	4.84217e-06
MYOG	[NCBI]	4.83568e-06
MMP1	[NCBI]	4.42791e-06
VCAN	[NCBI]	4.37774e-06
TFF2	[NCBI]	4.18563e-06
NME1	[NCBI]	4.0191e-06
TFF1	[NCBI]	3.86929e-06
IL1B	[NCBI]	3.77186e-06
MMP9	[NCBI]	3.73713e-06
TOP2A	[NCBI]	3.71187e-06
ABCG2	[NCBI]	3.5853e-06
CD68	[NCBI]	2.62498e-06
MS	[NCBI]	2.50506e-06
CDKN1A	[NCBI]	1.65919e-06
NPY	[NCBI]	1.57797e-06
EGF	[NCBI]	8.29856e-07

OMIM	Link	Information gain
HMN7A	[NCBI]	0.00321518
MPD2	[NCBI]	0.00137599
hereditary motor and sensory neuropathy, type iic	[NCBI]	0.0012742
laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy	[NCBI]	0.000246451
multiple pterygium syndrome, aslan type	[NCBI]	0.000207178
plasminogen deficiency, type i	[NCBI]	0.00016988
epidermolysis bullosa herpetiformis, dowling-meara type	[NCBI]	0.00016988
lipoid proteinosis of urbach and wiethe	[NCBI]	0.000142421
HGF	[NCBI]	0.000140777
MJD	[NCBI]	7.61832e-05
TTID	[NCBI]	4.66334e-05
PD	[NCBI]	4.64316e-05
KRT5	[NCBI]	3.76942e-05
KRT14	[NCBI]	3.76942e-05
EGFR	[NCBI]	3.49804e-05
PLG	[NCBI]	2.6549e-05
SDC2	[NCBI]	1.94108e-05
PCNA	[NCBI]	1.8727e-05
MUC1	[NCBI]	1.64973e-05
RA	[NCBI]	6.37899e-06
NPY	[NCBI]	2.50024e-06
SLE	[NCBI]	8.37634e-07
EGF	[NCBI]	3.47876e-08