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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ichthyosiform Erythroderma, Congenital [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science