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MeSH keywords -> Related genes, diseases (OMIM)


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01 Skin Diseases, Vesiculobullous [NCBI]

Gene


 Gene Link Information
Gain		 01
EBM [NCBI] 0.000438875
LAD1 [NCBI] 7.71574e-05
LAMB3 [NCBI] 6.82615e-05
DST [NCBI] 4.71762e-05
DSP [NCBI] 3.84337e-05
KRT2 [NCBI] 3.47457e-05
DSG3 [NCBI] 3.28139e-05
DSC1 [NCBI] 2.212e-05
KRT36 [NCBI] 1.6795e-05
CCL11 [NCBI] 1.18678e-05
IQGAP1 [NCBI] 1.03731e-05
PPL [NCBI] 1.01648e-05
CXCR7 [NCBI] 9.97915e-06
FERMT1 [NCBI] 9.58761e-06
COL17A1 [NCBI] 8.72597e-06
GNLY [NCBI] 8.12574e-06
KRT10 [NCBI] 7.75288e-06
MS [NCBI] 7.68417e-06
PLEC1 [NCBI] 7.65979e-06
TPMT [NCBI] 7.50821e-06
RPL22 [NCBI] 6.9785e-06
DSG1 [NCBI] 6.75169e-06
CX3CR1 [NCBI] 6.72536e-06
CXCL1 [NCBI] 5.34925e-06
IKBKE [NCBI] 5.32639e-06
CHUK [NCBI] 5.15403e-06
IKBKB [NCBI] 5.14383e-06
PAH [NCBI] 4.96113e-06
ERCC2 [NCBI] 4.86393e-06
GZMB [NCBI] 4.78438e-06
PIH [NCBI] 4.77623e-06
VIP [NCBI] 3.39283e-06
MPO [NCBI] 1.9803e-06
PTGS2 [NCBI] 1.22518e-06



OMIM


 OMIM Link Information
gain		 01
bullous dystrophy, hereditary macular type [NCBI] 0.00187142
basaloid follicular hamartoma syndrome, generalized, autosomal dominant [NCBI] 0.00114043
aplasia cutis congenita of limbs, recessive [NCBI] 0.00092257
malignant atrophic papulosis [NCBI] 0.000715905
actinic prurigo [NCBI] 0.000689681
peeling skin syndrome [NCBI] 0.000667246
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000572775
SLE [NCBI] 0.000381718
OCP [NCBI] 0.000302548
TBDN [NCBI] 0.000166112
epidermolysis bullosa letalis [NCBI] 0.000121273
RA [NCBI] 0.000104032
pachyonychia congenita, recessive [NCBI] 8.84101e-05
peeling skin syndrome, acral type [NCBI] 8.84101e-05
nevus, epidermal, epidermolytic hyperkeratotic type [NCBI] 8.84101e-05
zunich neuroectodermal syndrome [NCBI] 7.55723e-05
DSC1 [NCBI] 7.32984e-05
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 7.28681e-05
ichthyosis, bullous type [NCBI] 7.05545e-05
TGM5 [NCBI] 6.99214e-05
KRT2A [NCBI] 5.99713e-05
KRT10 [NCBI] 5.89764e-05
EPPK [NCBI] 5.78555e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 5.69116e-05
EPS [NCBI] 5.36147e-05
DST [NCBI] 5.28281e-05
PPOX [NCBI] 4.90631e-05
EBR1 [NCBI] 4.85676e-05
RNASE3 [NCBI] 4.57049e-05
mannosidosis, alpha b, lysosomal [NCBI] 4.51872e-05
RNASE2 [NCBI] 4.14464e-05
DSG3 [NCBI] 4.08236e-05
LSA [NCBI] 3.53086e-05
porphyria variegata [NCBI] 3.38028e-05
hla-d histocompatibility type [NCBI] 2.92554e-05
IP [NCBI] 2.48261e-05
VIP [NCBI] 1.50331e-05
MPO [NCBI] 7.59094e-06
CEACAM5 [NCBI] 3.41164e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.77213e-07
VEGF [NCBI] 4.33511e-07



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