Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hypohidrosis	[NCBI]

Gene	Link	Information Gain
EDA	[NCBI]	0.000107404
NTRK1	[NCBI]	9.85422e-05
EDAR	[NCBI]	9.82813e-05
MS	[NCBI]	5.28348e-05
NGF	[NCBI]	4.21606e-05
IKBKE	[NCBI]	1.44662e-05
CHUK	[NCBI]	1.41168e-05
IKBKB	[NCBI]	1.40961e-05
PKP1	[NCBI]	1.02922e-05
IKBKG	[NCBI]	8.12983e-06
EGF	[NCBI]	5.50866e-06
TP63	[NCBI]	5.39198e-06
MAPT	[NCBI]	4.92423e-06
G6PD	[NCBI]	4.2109e-06

OMIM	Link	Information gain
ED1	[NCBI]	0.00146908
CIPA	[NCBI]	0.00101341
BZX	[NCBI]	0.000832846
SHFM1	[NCBI]	0.000647409
NTRK1	[NCBI]	0.000386403
ED3	[NCBI]	0.00031298
anhidrosis, familial generalized, with normal sweat glands	[NCBI]	0.000244659
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia	[NCBI]	0.000244659
naegeli syndrome	[NCBI]	0.000176813
NGFB	[NCBI]	0.000166174
neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia	[NCBI]	0.000122157
hypohidrosis with abnormal palmar dermal ridges	[NCBI]	0.000122157
EDA	[NCBI]	0.000114234
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis	[NCBI]	9.96932e-05
ectodermal dysplasia/skin fragility syndrome	[NCBI]	7.83769e-05
DPR	[NCBI]	7.83769e-05
IP	[NCBI]	7.65692e-05
ankyloblepharon-ectodermal defects-cleft lip/palate	[NCBI]	6.79212e-05
adult syndrome	[NCBI]	6.51102e-05
EBS-MP	[NCBI]	6.51102e-05
LMS	[NCBI]	6.27202e-05
EDAR	[NCBI]	6.22784e-05
EEC3	[NCBI]	6.0642e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant	[NCBI]	5.96965e-05
RHS	[NCBI]	5.71567e-05
SLE	[NCBI]	5.3175e-05
TP73L	[NCBI]	4.74381e-05
KRT14	[NCBI]	4.70416e-05
IKBKG	[NCBI]	4.59395e-05
SJS1	[NCBI]	4.4445e-05
KSS	[NCBI]	2.57561e-05
G6PD	[NCBI]	1.17779e-05
EGF	[NCBI]	1.15893e-05
FTD	[NCBI]	7.28104e-06