Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Dermatitis, Exfoliative [NCBI]

Gene


 Gene Link Information
Gain		 01
KWE [NCBI] 0.000438875
SPINK5 [NCBI] 5.01252e-05
TGM1 [NCBI] 3.26739e-05
GJB4 [NCBI] 1.36815e-05
LOR [NCBI] 1.25575e-05
EBP [NCBI] 1.09706e-05
KIR2DL2 [NCBI] 1.04566e-05
ALDH3A2 [NCBI] 9.87939e-06
GJB3 [NCBI] 9.7678e-06
PTPRC [NCBI] 9.10436e-06
RAG2 [NCBI] 8.39443e-06
CCL17 [NCBI] 8.07524e-06
CCR4 [NCBI] 7.94019e-06
CXCR3 [NCBI] 6.74446e-06
RAG1 [NCBI] 6.65943e-06
GJB2 [NCBI] 5.79948e-06



OMIM


 OMIM Link Information
gain		 01
keratolytic winter erythema [NCBI] 0.00200072
erythroderma, lethal congenital [NCBI] 0.00119841
erythrokeratodermia variabilis 3 [NCBI] 0.000898321
trichohepatoenteric syndrome [NCBI] 0.000844965
EKV [NCBI] 0.000792262
complement component 5 deficiency [NCBI] 0.000418878
NETH [NCBI] 0.000164737
LOR [NCBI] 0.00014762
erythrokeratodermia, progressive symmetric [NCBI] 0.00013289
GJB3 [NCBI] 0.000126586
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000122444
ichthyosis, hystrix-like, with deafness [NCBI] 0.000110422
ichthyosis, x-linked [NCBI] 0.000101094
ichthyosis, bullous type [NCBI] 8.40597e-05
kindler syndrome [NCBI] 7.71411e-05
ichthyosis vulgaris [NCBI] 7.33947e-05
CDS [NCBI] 7.33947e-05
GJB4 [NCBI] 7.20115e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 7.03584e-05
omenn syndrome [NCBI] 6.94617e-05
ichthyosis congenita, harlequin fetus type [NCBI] 6.7806e-05
SPINK5 [NCBI] 6.26709e-05
CDPX2 [NCBI] 5.85232e-05
DKC [NCBI] 5.72558e-05
TGM1 [NCBI] 5.69272e-05
LI1 [NCBI] 5.33212e-05
GJB2 [NCBI] 3.65463e-05



Database Center for Life Science