Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Etretinate [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science