Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ichthyosiform Erythroderma, Congenital	[NCBI]

Gene	Link	Information Gain
SPINK5	[NCBI]	0.000312358
NEWENTRY	[NCBI]	0.000240374
TGM1	[NCBI]	0.000112265
KRT1	[NCBI]	3.112e-05
ALOX12B	[NCBI]	2.69966e-05
NSDHL	[NCBI]	2.36961e-05
ABHD5	[NCBI]	2.22153e-05
KRT10	[NCBI]	1.78678e-05
NPAL2	[NCBI]	1.67592e-05
ICHTHYIN	[NCBI]	1.43788e-05
ALOXE3	[NCBI]	1.34804e-05
CYP4F22	[NCBI]	1.34804e-05
NIPA2	[NCBI]	1.2897e-05
LOR	[NCBI]	1.07066e-05
TGM3	[NCBI]	9.94342e-06
ABCA12	[NCBI]	9.62335e-06
ALOX12	[NCBI]	9.17627e-06
SCN9A	[NCBI]	7.97499e-06
IKBKG	[NCBI]	7.39169e-06
GJB2	[NCBI]	3.99012e-06

OMIM	Link	Information gain
NNCI	[NCBI]	0.00115589
LI5	[NCBI]	0.00107364
peeling skin syndrome	[NCBI]	0.000900049
LI1	[NCBI]	0.000824283
NCIE1	[NCBI]	0.000628042
NETH	[NCBI]	0.000492236
SPINK5	[NCBI]	0.000291873
LI3	[NCBI]	0.000218924
KRT10	[NCBI]	0.000210686
bullous erythroderma ichthyosiformis congenita of brocq	[NCBI]	0.000200717
TGM1	[NCBI]	0.000189154
ALOXE3	[NCBI]	0.000182473
congenital hemidysplasia with ichthyosiform erythroderma and limb defects	[NCBI]	0.000170839
CDS	[NCBI]	0.000168437
ALOX12B	[NCBI]	0.000163492
KRT1	[NCBI]	0.000121277
nevus, epidermal, epidermolytic hyperkeratotic type	[NCBI]	0.000100673
LI2	[NCBI]	9.1078e-05
vohwinkel syndrome, variant form	[NCBI]	8.78187e-05
gaucher disease, perinatal lethal	[NCBI]	7.73439e-05
ichthyin	[NCBI]	7.71252e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant	[NCBI]	6.90923e-05
NSDHL	[NCBI]	6.40367e-05
LOR	[NCBI]	5.97044e-05
EKV	[NCBI]	5.96288e-05