Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Sweating	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	9.69443e-05
CRLF1	[NCBI]	1.31315e-05
VIP	[NCBI]	1.26947e-05
CFTR	[NCBI]	1.14277e-05
CLCF1	[NCBI]	8.13055e-06
CNTFR	[NCBI]	7.31239e-06
ACHE	[NCBI]	7.26002e-06
CNTF	[NCBI]	7.00156e-06
AVP	[NCBI]	3.06083e-06
PIP	[NCBI]	2.78756e-06
EWSR1	[NCBI]	2.77751e-06
PRL	[NCBI]	2.61184e-06
ATP7B	[NCBI]	2.58581e-06
LIFR	[NCBI]	2.35179e-06
GNAS	[NCBI]	2.26051e-06
IL6ST	[NCBI]	1.96529e-06
LIF	[NCBI]	1.4775e-06
EGF	[NCBI]	6.76479e-07

OMIM	Link	Information gain
ameloonychohypohidrotic syndrome	[NCBI]	0.00138218
fingerprints, absence of	[NCBI]	0.00138218
johnson neuroectodermal syndrome	[NCBI]	0.00111709
hyperpigmentation, familial progressive	[NCBI]	0.00111709
visceral neuropathy, familial, autosomal recessive	[NCBI]	0.000904017
megaduodenum and/or megacystis	[NCBI]	0.000833714
CIPA	[NCBI]	0.000417066
ED1	[NCBI]	0.000319147
SRS	[NCBI]	0.000292453
crisponi syndrome	[NCBI]	0.000262104
PC1	[NCBI]	0.000216502
CF	[NCBI]	0.000163549
BCPM	[NCBI]	0.000152094
CISS1	[NCBI]	0.000149925
anonychia with flexural pigmentation	[NCBI]	0.000149925
anhidrosis, familial generalized, with normal sweat glands	[NCBI]	0.000149925
CISS2	[NCBI]	0.000149925
CRLF1	[NCBI]	0.000131659
cerebellar ataxia and ectodermal dysplasia	[NCBI]	0.000122162
urticaria, aquagenic	[NCBI]	0.00011169
ectodermal dysplasia, anhidrotic	[NCBI]	9.24759e-05
stuve-wiedemann syndrome	[NCBI]	8.48958e-05
kindler syndrome	[NCBI]	8.48958e-05
VIP	[NCBI]	8.06989e-05
CNTFR	[NCBI]	7.70263e-05
HSAN2	[NCBI]	7.51489e-05
dopamine beta-hydroxylase deficiency, congenital	[NCBI]	7.3907e-05
pulmonary fibrosis, idiopathic	[NCBI]	6.86584e-05
SLS	[NCBI]	5.03893e-05
CNTF	[NCBI]	4.96926e-05
CLCF1	[NCBI]	4.36237e-05
MAS	[NCBI]	4.19372e-05
ACHE	[NCBI]	3.80165e-05
SLE	[NCBI]	3.67763e-05
EDA	[NCBI]	3.00176e-05
AVP	[NCBI]	2.3947e-05
PRL	[NCBI]	8.1208e-06
PD	[NCBI]	5.45602e-06
CFTR	[NCBI]	5.16493e-06
CEACAM5	[NCBI]	3.2985e-06
KLK3	[NCBI]	2.248e-06
VEGF	[NCBI]	2.54717e-08
EGF	[NCBI]	1.44494e-10