Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Back	[NCBI]

Gene	Link	Information Gain
AIS	[NCBI]	0.000422561
GER	[NCBI]	0.000102676
EN1	[NCBI]	7.10677e-06
OCA2	[NCBI]	6.93717e-06
MYO5A	[NCBI]	6.60783e-06
FABP2	[NCBI]	6.57109e-06
KRT10	[NCBI]	6.08178e-06
ATXN3	[NCBI]	5.6929e-06
FAAH	[NCBI]	5.44243e-06
TYRP1	[NCBI]	5.32695e-06
MITF	[NCBI]	5.05187e-06
BRAF	[NCBI]	4.80219e-06
MSH2	[NCBI]	4.67024e-06
GJB2	[NCBI]	4.42403e-06
MLH1	[NCBI]	4.34933e-06
MLL	[NCBI]	4.28168e-06
CTNNB1	[NCBI]	3.01849e-06
EPO	[NCBI]	2.83544e-06
MS	[NCBI]	2.50506e-06
EGFR	[NCBI]	2.44941e-06
ACHE	[NCBI]	2.43816e-06

OMIM	Link	Information gain
striae distensae, familial	[NCBI]	0.00158502
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality	[NCBI]	0.0012742
lethal congenital contracture syndrome 1	[NCBI]	0.00108094
IS1	[NCBI]	0.000953538
facial ectodermal dysplasia	[NCBI]	0.000835024
pena-shokeir syndrome, type i	[NCBI]	0.000614097
MTS	[NCBI]	0.000474418
halo nevi	[NCBI]	0.000235516
GPHN	[NCBI]	0.000196245
DFSP	[NCBI]	0.000192396
hypertrichosis, anterior cervical	[NCBI]	0.000181427
hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy	[NCBI]	0.000181427
schwannomatosis	[NCBI]	0.000158956
amyloidosis, primary cutaneous	[NCBI]	0.000126207
EBR1	[NCBI]	0.000119118
ED1	[NCBI]	9.87094e-05
glycogen storage disease ii	[NCBI]	8.87068e-05
FABP2	[NCBI]	5.17116e-05
FAAH	[NCBI]	3.33036e-05
ABP1	[NCBI]	3.22323e-05
EPO	[NCBI]	1.44618e-05
ACHE	[NCBI]	1.16136e-05