Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Etretinate	[NCBI]

Gene	Link	Information Gain
HFM	[NCBI]	0.00018904
FOP	[NCBI]	0.00013951
MS	[NCBI]	1.37638e-05
ACSL4	[NCBI]	2.51255e-06
ABCA12	[NCBI]	2.40177e-06
CRABP2	[NCBI]	2.39285e-06
DSC1	[NCBI]	2.24755e-06
TGM1	[NCBI]	1.90701e-06
CCR4	[NCBI]	1.81397e-06
TFRC	[NCBI]	1.64604e-06
G6PD	[NCBI]	1.41018e-06
LPL	[NCBI]	1.21858e-06

OMIM	Link	Information gain
sclerotylosis	[NCBI]	0.00277021
HLP	[NCBI]	0.00182656
HFM	[NCBI]	0.00163383
EV	[NCBI]	0.000366787
KFSD	[NCBI]	0.000260794
EKV	[NCBI]	0.000226723
BCNS	[NCBI]	0.0001588
ichthyosiform erythroderma, corneal involvement, and deafness	[NCBI]	0.000155135
ichthyosis, bullous type	[NCBI]	0.000125145
deafness, congenital, with keratopachydermia and constrictions of fingers and toes	[NCBI]	0.000118075
keratitis-ichthyosis-deafness syndrome, autosomal dominant	[NCBI]	0.000118075
ichthyosis congenita, harlequin fetus type	[NCBI]	0.000108349
LSA	[NCBI]	8.77658e-05
FOP	[NCBI]	8.21764e-05
BCPM	[NCBI]	8.09729e-05
bullous erythroderma ichthyosiformis congenita of brocq	[NCBI]	7.67194e-05
RBP1	[NCBI]	2.79671e-05
RNASE3	[NCBI]	1.81517e-05
G6PD	[NCBI]	1.64848e-05
LPL	[NCBI]	1.35313e-05