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MeSH keywords -> Related genes, diseases (OMIM)


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01 Epidermolysis Bullosa [NCBI]

Gene


 Gene Link Information
Gain		 01
LAMB3 [NCBI] 0.000167991
PLEC1 [NCBI] 0.000151493
ITGB4 [NCBI] 0.000100352
COL7A1 [NCBI] 8.53441e-05
COL17A1 [NCBI] 8.09962e-05
KRT14 [NCBI] 4.30277e-05
LAMC2 [NCBI] 3.57622e-05
NID1 [NCBI] 2.46834e-05
EIF6 [NCBI] 1.09179e-05
KRT15 [NCBI] 1.05118e-05
COL15A1 [NCBI] 1.05118e-05
SLC39A4 [NCBI] 9.46338e-06
LAMA3 [NCBI] 9.2778e-06
DSC2 [NCBI] 9.2778e-06
KRT9 [NCBI] 9.19205e-06
DSC1 [NCBI] 9.1104e-06
LAMA5 [NCBI] 8.81794e-06
CD151 [NCBI] 7.94316e-06
PPOX [NCBI] 6.72922e-06
DSP [NCBI] 6.4568e-06
KRT5 [NCBI] 6.10941e-06
TP63 [NCBI] 4.01959e-06
PTK2 [NCBI] 3.59796e-06
ACHE [NCBI] 2.27151e-06
CD68 [NCBI] 2.13224e-06
AFP [NCBI] 1.36573e-06



OMIM


 OMIM Link Information
gain		 01
epidermolysis bullosa inversa dystrophica [NCBI] 0.00183628
EBR1 [NCBI] 0.0017621
EBS2 [NCBI] 0.00125087
epidermolysis bullosa letalis [NCBI] 0.00120287
epidermolysis bullosa with pyloric atresia [NCBI] 0.00111518
amelogenesis imperfecta, hypoplastic type [NCBI] 0.000866698
bullous dystrophy, hereditary macular type [NCBI] 0.000813359
sclerotylosis [NCBI] 0.000715905
epidermolysis bullosa dystrophica, pasini type [NCBI] 0.000643535
epidermolysis bullosa simplex and limb-girdle muscular dystrophy [NCBI] 0.00057383
GABEB [NCBI] 0.000531537
epidermolysis bullosa with congenital localized absence of skin and deformity of nails [NCBI] 0.000474509
AOS [NCBI] 0.000431032
kindler syndrome [NCBI] 0.000410374
COL17A1 [NCBI] 0.000356797
epidermolysis bullosa herpetiformis, dowling-meara type [NCBI] 0.000333467
COL7A1 [NCBI] 0.000332574
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 0.000288531
epidermolysis bullosa of hands and feet [NCBI] 0.000257617
TBDN [NCBI] 0.00023928
epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase [NCBI] 0.000216504
nephropathy with pretibial epidermolysis bullosa and deafness [NCBI] 0.000216504
raph blood group system [NCBI] 0.00018557
ITGB4 [NCBI] 0.000180247
epidermolysis bullosa simplex, ogna type [NCBI] 0.000171599
EBDSC [NCBI] 0.000162015
SLE [NCBI] 0.000136396
PLEC1 [NCBI] 0.000130073
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000129898
EBS-MP [NCBI] 0.000126252
epidermolysis bullosa simplex, autosomal recessive [NCBI] 0.00010818
epidermolysis bullosa with diaphragmatic hernia [NCBI] 0.00010818
epidermolysis bullosa, lethal acantholytic [NCBI] 0.00010818
LAMB3 [NCBI] 0.000100524
GPT [NCBI] 8.31014e-05
pachyonychia congenita, recessive [NCBI] 7.72659e-05
ichthyosis hystrix gravior [NCBI] 7.72659e-05
epidermolysis bullosa, pretibial [NCBI] 7.1778e-05
LOCS [NCBI] 7.1778e-05
keratitis, hereditary [NCBI] 6.77024e-05
NID [NCBI] 6.48763e-05
ITGA6 [NCBI] 6.48763e-05
CD151 [NCBI] 6.48763e-05
mental retardation, fra12a type [NCBI] 6.44587e-05
TGM5 [NCBI] 6.15005e-05
IHCM [NCBI] 5.74502e-05
AIH2 [NCBI] 5.74502e-05
LAMC2 [NCBI] 5.5329e-05
LAMA3 [NCBI] 5.39062e-05
ichthyosis vulgaris [NCBI] 4.89087e-05
tight skin contracture syndrome, lethal [NCBI] 4.68542e-05
KRT9 [NCBI] 4.67012e-05
DSP [NCBI] 4.60816e-05
ichthyosis congenita, harlequin fetus type [NCBI] 4.34163e-05
KRT14 [NCBI] 4.17725e-05
KRT5 [NCBI] 4.06731e-05
OCA1A [NCBI] 3.20455e-05
SDC2 [NCBI] 2.4454e-05
ACHE [NCBI] 5.48432e-06
AFP [NCBI] 1.81877e-06



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