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MeSH keywords -> Related genes, diseases (OMIM)


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01 Skin Diseases [NCBI]


Gene


Gene Link Information
Gain
01
PDR [NCBI] 0.000352784
DUH [NCBI] 0.000243202
KTWS [NCBI] 0.000186344
WG [NCBI] 0.000136929
CD68 [NCBI] 0.000125519
FOP [NCBI] 0.000125287
UROD [NCBI] 7.40359e-05
PPOX [NCBI] 6.58443e-05
PKP1 [NCBI] 6.43366e-05
MS [NCBI] 6.28963e-05
TROVE2 [NCBI] 4.33996e-05
HR [NCBI] 3.71904e-05
ANTXR2 [NCBI] 3.45015e-05
DSG3 [NCBI] 2.94659e-05
DSG1 [NCBI] 2.79031e-05
CTAGE1 [NCBI] 2.72596e-05
FLCN [NCBI] 2.67122e-05
NLRP3 [NCBI] 2.66048e-05
KRT14 [NCBI] 2.65478e-05
GJB3 [NCBI] 2.56433e-05
KRT17 [NCBI] 2.39526e-05
LAMB3 [NCBI] 2.39282e-05
LMNA [NCBI] 2.19606e-05
ABCC6 [NCBI] 2.19384e-05
KLK7 [NCBI] 2.04654e-05
GJB2 [NCBI] 1.90695e-05
GJB4 [NCBI] 1.84455e-05
CCL11 [NCBI] 1.79157e-05
S100A7A [NCBI] 1.79128e-05
PCNA [NCBI] 1.76392e-05
PLEC1 [NCBI] 1.6826e-05
LOR [NCBI] 1.60588e-05
HOXB4 [NCBI] 1.55303e-05
DSP [NCBI] 1.53092e-05
CTGF [NCBI] 1.48876e-05
KRT5 [NCBI] 1.42701e-05
KLK5 [NCBI] 1.36871e-05
KLK8 [NCBI] 1.36871e-05
FERMT1 [NCBI] 1.36871e-05
CXCR3 [NCBI] 1.36739e-05
ERCC2 [NCBI] 1.33319e-05
PKP2 [NCBI] 1.32854e-05
GSTO1 [NCBI] 1.30418e-05
PI3 [NCBI] 1.29263e-05
FABP5 [NCBI] 1.28146e-05
AADACL2 [NCBI] 1.28142e-05
LIPN [NCBI] 1.28142e-05
LIPM [NCBI] 1.28142e-05
MPZL3 [NCBI] 1.28142e-05
KRT71 [NCBI] 1.28142e-05
LIPK [NCBI] 1.28142e-05
PNPLA1 [NCBI] 1.28142e-05
SIGLEC15 [NCBI] 1.28142e-05
CCL17 [NCBI] 1.26841e-05
ERCC8 [NCBI] 1.24017e-05
GNAS [NCBI] 1.17033e-05
XPA [NCBI] 1.16556e-05
EGF [NCBI] 1.10792e-05
TAP2 [NCBI] 1.10132e-05
SPINK5 [NCBI] 1.07481e-05
FLG [NCBI] 1.06893e-05
A2ML1 [NCBI] 1.04346e-05
ICHTHYIN [NCBI] 1.04346e-05
IFFO1 [NCBI] 1.04346e-05
CCDC66 [NCBI] 1.04346e-05
NLRP4 [NCBI] 1.04346e-05
CKMT2 [NCBI] 1.04346e-05
C1orf68 [NCBI] 1.04346e-05
STAB2 [NCBI] 1.04346e-05
S100A7 [NCBI] 1.02027e-05
TNF [NCBI] 1.01405e-05
KRT10 [NCBI] 1.00075e-05
NR1H3 [NCBI] 9.81473e-06
NOD2 [NCBI] 9.689e-06
CKMT1A [NCBI] 9.53712e-06
TGM5 [NCBI] 9.53712e-06
PLA2G4B [NCBI] 9.53712e-06
TMEM159 [NCBI] 9.53712e-06
MGAT4C [NCBI] 9.53712e-06
TLR7 [NCBI] 9.36395e-06
GJB6 [NCBI] 9.32523e-06
POMC [NCBI] 9.18827e-06
ICAM3 [NCBI] 9.06633e-06
SPRR1A [NCBI] 8.95461e-06
RNASE7 [NCBI] 8.95461e-06
ERCC6 [NCBI] 8.60327e-06
B2M [NCBI] 8.5726e-06
GTF2H5 [NCBI] 8.52171e-06
ARHGAP6 [NCBI] 8.52171e-06
C6orf142 [NCBI] 8.52171e-06
SH2D3C [NCBI] 8.52171e-06
EMCN [NCBI] 8.52171e-06
PADI3 [NCBI] 8.52171e-06
CKMT1B [NCBI] 8.52171e-06
CCR6 [NCBI] 8.36572e-06
CCL20 [NCBI] 8.36572e-06
GSTM1 [NCBI] 8.243e-06
CD200R1 [NCBI] 8.17694e-06
IL1F6 [NCBI] 8.17694e-06
AS3MT [NCBI] 8.17694e-06
CLCN4 [NCBI] 8.17694e-06
GSTP1 [NCBI] 8.02821e-06
PADI1 [NCBI] 7.89039e-06
SAMD9 [NCBI] 7.89039e-06
TYRP1 [NCBI] 7.83909e-06
TSC2 [NCBI] 7.69673e-06
TST [NCBI] 7.64522e-06
DEFB4 [NCBI] 7.58279e-06
MMP21 [NCBI] 7.431e-06
CA3 [NCBI] 7.431e-06
CD200 [NCBI] 7.431e-06
FUT4 [NCBI] 7.431e-06
EGFR [NCBI] 7.34449e-06
SPRR1B [NCBI] 7.24079e-06
GTF2H4 [NCBI] 7.24079e-06
LPIN2 [NCBI] 7.06977e-06
GTF2H2 [NCBI] 7.06977e-06
GSTO2 [NCBI] 6.91444e-06
PADI2 [NCBI] 6.91444e-06
KLK14 [NCBI] 6.91444e-06
FUT7 [NCBI] 6.91444e-06
LCN2 [NCBI] 6.90166e-06
CCR4 [NCBI] 6.84816e-06
GPR109B [NCBI] 6.77216e-06
KRT6B [NCBI] 6.64092e-06
GBP1 [NCBI] 6.64092e-06
DPP4 [NCBI] 6.54532e-06
LEMD3 [NCBI] 6.51915e-06
KLK13 [NCBI] 6.51915e-06
EXOSC10 [NCBI] 6.51915e-06
GALNT3 [NCBI] 6.51915e-06
AREG [NCBI] 6.4198e-06
DSG4 [NCBI] 6.40557e-06
FLII [NCBI] 6.40557e-06
ETS1 [NCBI] 6.40447e-06
NME1 [NCBI] 6.30518e-06
MCM5 [NCBI] 6.10462e-06
NR1H2 [NCBI] 6.10462e-06
OCLN [NCBI] 6.01519e-06
DCD [NCBI] 6.01519e-06
CCNH [NCBI] 6.01519e-06
TRAF1 [NCBI] 6.01519e-06
KRT16 [NCBI] 5.93028e-06
LDLRAP1 [NCBI] 5.93028e-06
ABHD5 [NCBI] 5.93028e-06
ACADM [NCBI] 5.93028e-06
CST6 [NCBI] 5.84946e-06
DSC1 [NCBI] 5.84946e-06
CCR7 [NCBI] 5.7724e-06
SOS1 [NCBI] 5.77237e-06
XBP1 [NCBI] 5.77237e-06
GSTT1 [NCBI] 5.73354e-06
MMP10 [NCBI] 5.69867e-06
ABCA12 [NCBI] 5.69867e-06
BCAM [NCBI] 5.69867e-06
NME2 [NCBI] 5.69867e-06
CCL2 [NCBI] 5.64897e-06
TBX21 [NCBI] 5.62809e-06
ZMPSTE24 [NCBI] 5.56037e-06
FSCN1 [NCBI] 5.56037e-06
HOXB13 [NCBI] 5.56037e-06
CCR10 [NCBI] 5.49529e-06
PDPN [NCBI] 5.43266e-06
CCL27 [NCBI] 5.43266e-06
LTBP1 [NCBI] 5.37231e-06
TRPC6 [NCBI] 5.31407e-06
CTSG [NCBI] 5.30439e-06
PTEN [NCBI] 5.27678e-06
HBEGF [NCBI] 5.2578e-06
KIF11 [NCBI] 5.20339e-06
CD207 [NCBI] 5.20339e-06
TAP1 [NCBI] 5.17053e-06
GCNT1 [NCBI] 5.09964e-06
CDSN [NCBI] 5.00203e-06
LTB [NCBI] 5.00203e-06
MCM7 [NCBI] 4.95531e-06
CD247 [NCBI] 4.90988e-06
CD55 [NCBI] 4.90988e-06
XCL1 [NCBI] 4.86568e-06
DSG2 [NCBI] 4.86568e-06
IL1A [NCBI] 4.86566e-06
MMP26 [NCBI] 4.82263e-06
PDCD4 [NCBI] 4.69987e-06
TAC1 [NCBI] 4.66092e-06
ECM1 [NCBI] 4.62288e-06
TNFRSF18 [NCBI] 4.5138e-06
PRKD1 [NCBI] 4.47901e-06
APC [NCBI] 4.47285e-06
CD28 [NCBI] 4.3789e-06
KLK6 [NCBI] 4.3789e-06
IL2 [NCBI] 4.3786e-06
LOX [NCBI] 4.34686e-06
GZMB [NCBI] 4.3188e-06
NOV [NCBI] 4.31544e-06
CDK7 [NCBI] 4.28463e-06
UCN [NCBI] 4.28463e-06
TEP1 [NCBI] 4.25439e-06
CLC [NCBI] 4.19557e-06
PLEK [NCBI] 4.19557e-06
IL3RA [NCBI] 4.19557e-06
IRF2 [NCBI] 4.16695e-06
TNFSF8 [NCBI] 4.16695e-06
L1CAM [NCBI] 4.13883e-06
KLRC1 [NCBI] 4.00519e-06
PPARD [NCBI] 4.00519e-06
GSTM3 [NCBI] 3.93008e-06
CCL19 [NCBI] 3.88191e-06
TSC1 [NCBI] 3.88191e-06
HMBS [NCBI] 3.85837e-06
CXCL13 [NCBI] 3.83517e-06
FGFR3 [NCBI] 3.79742e-06
S100A6 [NCBI] 3.78976e-06
COL7A1 [NCBI] 3.72402e-06
RAGE [NCBI] 3.70271e-06
DKC1 [NCBI] 3.64045e-06
TPMT [NCBI] 3.60027e-06
KLF4 [NCBI] 3.60027e-06
TTR [NCBI] 3.56071e-06
PTX3 [NCBI] 3.52291e-06
TNFRSF4 [NCBI] 3.44923e-06
MC1R [NCBI] 3.44923e-06
BMP2 [NCBI] 3.40595e-06
GADD45A [NCBI] 3.32819e-06
SELP [NCBI] 3.31166e-06
EBAG9 [NCBI] 3.2953e-06
EDA [NCBI] 3.26309e-06
CCL21 [NCBI] 3.23156e-06
CYR61 [NCBI] 3.21603e-06
TGM1 [NCBI] 3.18545e-06
GZMA [NCBI] 3.1407e-06
MMP12 [NCBI] 3.12608e-06
NID1 [NCBI] 3.12608e-06
ACVRL1 [NCBI] 3.09725e-06
TGM2 [NCBI] 3.09725e-06
PPARA [NCBI] 3.09725e-06
F13A1 [NCBI] 3.08304e-06
FOXP3 [NCBI] 3.06896e-06
MPZ [NCBI] 3.06896e-06
PREPL [NCBI] 3.0275e-06
SFN [NCBI] 3.01394e-06
APRT [NCBI] 3.00049e-06
GATA3 [NCBI] 2.9479e-06
TRPV1 [NCBI] 2.92228e-06
IL2RA [NCBI] 2.8971e-06
EPB41L1 [NCBI] 2.88467e-06
RBL2 [NCBI] 2.86012e-06
TIA1 [NCBI] 2.78885e-06
PAX5 [NCBI] 2.75447e-06
RAG2 [NCBI] 2.732e-06
EPB41L2 [NCBI] 2.72089e-06
MMP7 [NCBI] 2.70987e-06
NGFR [NCBI] 2.70987e-06
TAT [NCBI] 2.70987e-06
ERCC5 [NCBI] 2.6773e-06
PIP [NCBI] 2.6666e-06
SRC [NCBI] 2.63498e-06
IL1RN [NCBI] 2.6077e-06
PTGS1 [NCBI] 2.56499e-06
MGP [NCBI] 2.51508e-06
SPN [NCBI] 2.50553e-06
PDCD1 [NCBI] 2.50553e-06
PMS2 [NCBI] 2.46797e-06
TP73 [NCBI] 2.45873e-06
CXCL9 [NCBI] 2.43138e-06
IGF1R [NCBI] 2.40456e-06
ADA [NCBI] 2.33218e-06
STAT6 [NCBI] 2.31043e-06
SAT2 [NCBI] 2.31043e-06
BCL6 [NCBI] 2.26168e-06
APOA1 [NCBI] 2.21462e-06
MITF [NCBI] 2.16914e-06
PTHLH [NCBI] 2.15831e-06
PIK3CA [NCBI] 2.15432e-06
CXCL10 [NCBI] 2.14697e-06
SOCS3 [NCBI] 2.14697e-06
XPC [NCBI] 2.13966e-06
DCT [NCBI] 2.11082e-06
BMP4 [NCBI] 2.00794e-06
HLA-C [NCBI] 2.00136e-06
SELPLG [NCBI] 1.96258e-06
VIP [NCBI] 1.96173e-06
APOD [NCBI] 1.94361e-06
FABP7 [NCBI] 1.88835e-06
CD44 [NCBI] 1.82392e-06
BAK1 [NCBI] 1.7957e-06
TJP1 [NCBI] 1.74647e-06
FGF23 [NCBI] 1.7252e-06
TGFB1 [NCBI] 1.67152e-06
CXCL1 [NCBI] 1.62901e-06
HLA-DRB1 [NCBI] 1.6107e-06
TNFRSF10A [NCBI] 1.57667e-06
MMP13 [NCBI] 1.53104e-06
XRCC5 [NCBI] 1.4574e-06
CAT [NCBI] 1.40445e-06
BCL2L1 [NCBI] 1.39141e-06
GAPDH [NCBI] 1.38043e-06
HP [NCBI] 1.33446e-06
PF4 [NCBI] 1.31586e-06
HLA-A [NCBI] 1.29397e-06
ALK [NCBI] 1.26195e-06
KRT7 [NCBI] 1.2515e-06
WAS [NCBI] 1.2343e-06
RAG1 [NCBI] 1.2343e-06
MTHFR [NCBI] 1.20717e-06
GJB1 [NCBI] 1.20404e-06
CYP1A1 [NCBI] 1.16505e-06
TP63 [NCBI] 1.10328e-06
IL4 [NCBI] 1.03958e-06
CCR2 [NCBI] 1.03678e-06
PKD1 [NCBI] 1.02844e-06
ENG [NCBI] 1.02568e-06
HLA-B [NCBI] 9.79923e-07
KRT20 [NCBI] 9.66891e-07
CTSL1 [NCBI] 9.06859e-07
PTGS2 [NCBI] 8.97761e-07
CHEK1 [NCBI] 8.94854e-07
CD86 [NCBI] 8.92473e-07
MUC1 [NCBI] 8.69021e-07
IL8 [NCBI] 8.69021e-07
NOS2 [NCBI] 8.2707e-07
APOE [NCBI] 8.10201e-07
MMP9 [NCBI] 7.91782e-07
PTK2 [NCBI] 7.87583e-07
PPARG [NCBI] 7.6082e-07
RET [NCBI] 7.19455e-07
CHAT [NCBI] 6.37924e-07
TNFRSF11A [NCBI] 6.01271e-07
LIF [NCBI] 5.85252e-07
BRAF [NCBI] 5.17766e-07
CTNNB1 [NCBI] 5.14739e-07
TNFSF11 [NCBI] 4.58405e-07
TNFRSF11B [NCBI] 4.34606e-07
CXCL12 [NCBI] 3.86691e-07
CDKN1A [NCBI] 3.8157e-07
CASP3 [NCBI] 3.59563e-07
G6PD [NCBI] 3.29136e-07
VWF [NCBI] 3.15367e-07
PLAUR [NCBI] 2.40683e-07
TRH [NCBI] 2.03317e-07
VEGFA [NCBI] 1.83437e-07
TP53 [NCBI] 1.80191e-07
ACE [NCBI] 1.76389e-07
HRAS [NCBI] 1.29987e-07
MSH2 [NCBI] 8.7548e-08
MPO [NCBI] 8.43389e-08
TH [NCBI] 8.36409e-08
HFE [NCBI] 7.79855e-08
ACHE [NCBI] 7.18672e-08
FASLG [NCBI] 6.4526e-08
TNFSF10 [NCBI] 5.00506e-08
AR [NCBI] 4.96068e-08
NOS3 [NCBI] 3.75431e-08
BAX [NCBI] 3.67557e-08
PTH [NCBI] 3.24519e-08
NPY [NCBI] 8.9568e-09
MBP [NCBI] 4.62884e-09
HGF [NCBI] 2.1998e-09




OMIM


OMIM Link Information
gain
01
peeling skin syndrome [NCBI] 0.00297688
sneddon syndrome [NCBI] 0.00297688
collagenosis, familial reactive perforating [NCBI] 0.00264781
BZX [NCBI] 0.00253238
malignant atrophic papulosis [NCBI] 0.00244196
neutrophilic dermatosis, acute febrile [NCBI] 0.0023163
comedones, familial dyskeratotic [NCBI] 0.00192434
stiff skin syndrome [NCBI] 0.001325
amyloidosis, primary cutaneous [NCBI] 0.00125251
PDR [NCBI] 0.00121674
LSA [NCBI] 0.00112893
sebaceous gland hyperplasia, familial presenile [NCBI] 0.0010823
dermochondrocorneal dystrophy [NCBI] 0.000990409
tight skin contracture syndrome, lethal [NCBI] 0.000970083
porphyria cutanea tarda [NCBI] 0.000909476
EPS [NCBI] 0.000788803
erythrokeratodermia with ataxia [NCBI] 0.000756802
striae distensae, familial [NCBI] 0.000756802
ameloonychohypohidrotic syndrome [NCBI] 0.000756802
basaloid follicular hamartoma syndrome, generalized, autosomal dominant [NCBI] 0.000756802
flynn-aird syndrome [NCBI] 0.000756802
borrone dermatocardioskeletal syndrome [NCBI] 0.000756802
EV [NCBI] 0.000717046
DKC [NCBI] 0.000639848
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.000628068
proteus syndrome [NCBI] 0.000577283
nail dysplasia [NCBI] 0.000540115
CMTC [NCBI] 0.000539973
RA [NCBI] 0.0005286
dubowitz syndrome [NCBI] 0.000461033
hyperimmunoglobulin e-recurrent infection syndrome, autosomal recessive [NCBI] 0.000459121
mucoepithelial dysplasia, hereditary [NCBI] 0.000459121
PN [NCBI] 0.000459121
erythrokeratodermia variabilis 3 [NCBI] 0.000459121
pigmented purpuric eruption [NCBI] 0.000459121
FDH [NCBI] 0.000412633
onychotrichodysplasia and neutropenia [NCBI] 0.00040697
acromial dimples [NCBI] 0.00040697
focal facial dermal dysplasia [NCBI] 0.00040697
telangiectasia, hereditary benign [NCBI] 0.00040697
TRICY1 [NCBI] 0.00040697
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.000338133
PPPP [NCBI] 0.000338133
SPG23 [NCBI] 0.00031308
AOS [NCBI] 0.000308379
PXE [NCBI] 0.000287122
porphyria cutanea tarda, type i [NCBI] 0.000266739
dermatitis, atopic [NCBI] 0.000257155
BHD [NCBI] 0.000236307
porphyria variegata [NCBI] 0.000229181
kindler syndrome [NCBI] 0.000220814
RTS [NCBI] 0.000211103
EKV [NCBI] 0.000207424
facial ectodermal dysplasia [NCBI] 0.000206969
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 0.000199102
ectodermal dysplasia/skin fragility syndrome [NCBI] 0.000190762
CD [NCBI] 0.000181569
KRT17 [NCBI] 0.000181255
IP [NCBI] 0.000164745
MTS [NCBI] 0.000146748
peeling skin syndrome, acral type [NCBI] 0.000141048
pachyonychia congenita, recessive [NCBI] 0.000141048
fountain syndrome [NCBI] 0.000141048
NETH [NCBI] 0.000127677
LOCS [NCBI] 0.000127139
cardiomyopathy-hypogonadism-collagenoma syndrome [NCBI] 0.000127139
MEN2A [NCBI] 0.000124717
coffin-siris syndrome [NCBI] 0.000117489
AIC [NCBI] 0.000117489
DDD [NCBI] 0.000117419
steatocystoma multiplex [NCBI] 0.000110336
dyschromatosis symmetrica hereditaria 1 [NCBI] 0.0001054
TGM5 [NCBI] 0.000100912
PKP1 [NCBI] 0.000100912
thrombocytopenia-absent radius syndrome [NCBI] 0.000100492
PC2 [NCBI] 9.52057e-05
dyskeratosis congenita, autosomal dominant [NCBI] 9.14499e-05
DSAP1 [NCBI] 9.14499e-05
poland syndrome [NCBI] 8.9573e-05
pseudoatrophoderma colli [NCBI] 8.5943e-05
cutis verticis gyrata, thyroid aplasia, and mental retardation [NCBI] 8.5943e-05
exostoses with anetodermia and brachydactyly, type e [NCBI] 8.5943e-05
vasculitis, lymphocytic, nodular [NCBI] 8.5943e-05
metaphyseal modeling abnormality, skin lesions, and spastic paraplegia [NCBI] 8.5943e-05
macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance [NCBI] 8.5943e-05
aplasia cutis congenita with intestinal lymphangiectasia [NCBI] 8.5943e-05
arthropathy, erosive [NCBI] 8.5943e-05
knuckle pads [NCBI] 8.5943e-05
skin fragility-woolly hair syndrome [NCBI] 8.5943e-05
WSS [NCBI] 8.50832e-05
XPF [NCBI] 8.50832e-05
HMI [NCBI] 8.31498e-05
LOR [NCBI] 8.11601e-05
congenital hemidysplasia with ichthyosiform erythroderma and limb defects [NCBI] 7.98158e-05
PC1 [NCBI] 7.98158e-05
protoporphyria, erythropoietic [NCBI] 7.94691e-05
LDHA [NCBI] 7.48507e-05
pseudoxanthoma elasticum, forme fruste [NCBI] 7.33152e-05
pena-shokeir syndrome, type i [NCBI] 7.13373e-05
buschke-ollendorff syndrome [NCBI] 6.79796e-05
TTDP [NCBI] 6.79796e-05
DSP [NCBI] 6.74642e-05
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 6.65521e-05
PDP [NCBI] 6.63959e-05
CLCN4 [NCBI] 6.41994e-05
MPZL3 [NCBI] 6.41994e-05
KRT15 [NCBI] 6.41994e-05
PAI2 [NCBI] 6.41994e-05
PI3 [NCBI] 6.40903e-05
ABSD [NCBI] 6.35512e-05
fascial dystrophy, congenital [NCBI] 6.35512e-05
coxoauricular syndrome [NCBI] 6.35512e-05
AMVC [NCBI] 6.35512e-05
acroosteolysis [NCBI] 6.35512e-05
poikiloderma, hereditary sclerosing [NCBI] 6.35512e-05
skeletal dysplasia with telangiectases and mesodermal dysgenesis of the iris [NCBI] 6.35512e-05
pellagra-like syndrome [NCBI] 6.35512e-05
hyaluronan metabolism, defect in [NCBI] 6.35512e-05
rombo syndrome [NCBI] 6.35512e-05
tracheobronchomegaly [NCBI] 6.35512e-05
MCOPCT3 [NCBI] 6.35512e-05
PEPD [NCBI] 6.30851e-05
LMNA [NCBI] 6.17595e-05
PLOD1 [NCBI] 6.12198e-05
lipoid proteinosis of urbach and wiethe [NCBI] 6.08036e-05
GJB3 [NCBI] 6.03509e-05
MADA [NCBI] 5.95601e-05
porphyria, congenital erythropoietic [NCBI] 5.95601e-05
KRT14 [NCBI] 5.87232e-05
epidermolysis bullosa with pyloric atresia [NCBI] 5.83686e-05
steatocystoma multiplex with natal teeth [NCBI] 5.515e-05
keratosis pilaris [NCBI] 5.515e-05
NFTC [NCBI] 5.515e-05
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency [NCBI] 5.515e-05
NS4 [NCBI] 5.515e-05
LDHCP [NCBI] 5.515e-05
syringomas, multiple [NCBI] 5.515e-05
muscular dystrophy, hemizygous lethal type [NCBI] 5.515e-05
HFTC [NCBI] 5.405e-05
thrombocytopenic purpura, autoimmune [NCBI] 5.34861e-05
ABCC6 [NCBI] 5.33252e-05
MCOPS7 [NCBI] 5.21184e-05
EXOSC10 [NCBI] 5.04342e-05
KRT6B [NCBI] 5.04342e-05
ichthyin [NCBI] 5.04342e-05
ARHGAP6 [NCBI] 5.04342e-05
acrogeria, gottron type [NCBI] 4.97225e-05
glomerulonephritis with sparse hair and telangiectases [NCBI] 4.97225e-05
PKDTS [NCBI] 4.97225e-05
dyskeratosis congenita, autosomal recessive [NCBI] 4.97225e-05
majeed syndrome [NCBI] 4.97225e-05
periodic fever, familial, autosomal dominant [NCBI] 4.86215e-05
RCDP1 [NCBI] 4.86215e-05
OCA2 [NCBI] 4.70297e-05
GJB2 [NCBI] 4.685e-05
melanosis, neurocutaneous [NCBI] 4.57075e-05
cutis gyrata syndrome of beare and stevenson [NCBI] 4.57075e-05
angioma serpiginosum, autosomal dominant [NCBI] 4.57075e-05
gastritis, familial giant hypertrophic [NCBI] 4.57075e-05
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 4.57075e-05
cardiofaciocutaneous syndrome [NCBI] 4.55278e-05
GTF2H5 [NCBI] 4.52483e-05
ITPKC [NCBI] 4.52483e-05
ANTXR2 [NCBI] 4.52483e-05
TGFA [NCBI] 4.52483e-05
SAMD9 [NCBI] 4.52483e-05
SDC4 [NCBI] 4.52483e-05
APOA1 [NCBI] 4.49476e-05
B2M [NCBI] 4.31655e-05
BJS [NCBI] 4.25243e-05
hyalinosis, infantile systemic [NCBI] 4.25243e-05
vohwinkel syndrome, variant form [NCBI] 4.25243e-05
pilomatrixoma [NCBI] 4.25243e-05
cleft, median, of upper lip with polyps of facial skin and nasal mucosa [NCBI] 4.25243e-05
TRAF1 [NCBI] 4.1886e-05
kindlin 1 [NCBI] 4.1886e-05
CCL17 [NCBI] 4.0932e-05
TS [NCBI] 4.03722e-05
fabry disease [NCBI] 4.02824e-05
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 3.98908e-05
epidermolysis bullosa with congenital localized absence of skin and deformity of nails [NCBI] 3.98908e-05
CINCA [NCBI] 3.98908e-05
TTDN1 [NCBI] 3.98908e-05
ADCC [NCBI] 3.98908e-05
NN [NCBI] 3.98908e-05
GJB4 [NCBI] 3.93899e-05
TNFRSF8 [NCBI] 3.93899e-05
KLK5 [NCBI] 3.93899e-05
CST6 [NCBI] 3.93899e-05
SOS1 [NCBI] 3.93899e-05
LI1 [NCBI] 3.90995e-05
CSA [NCBI] 3.79893e-05
VEGF [NCBI] 3.77215e-05
melorheostosis [NCBI] 3.76479e-05
TTDN1 [NCBI] 3.74038e-05
KLK3 [NCBI] 3.61863e-05
RXRA [NCBI] 3.57548e-05
DCD [NCBI] 3.57548e-05
KRT16 [NCBI] 3.57548e-05
IRF2 [NCBI] 3.57548e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 3.44596e-05
LPIN2 [NCBI] 3.43454e-05
ATP2C1 [NCBI] 3.43454e-05
ERCC4 [NCBI] 3.43454e-05
monilethrix [NCBI] 3.39732e-05
PDCD4 [NCBI] 3.31152e-05
GALNT3 [NCBI] 3.31152e-05
megalencephaly-cutis marmorata telangiectatica congenita [NCBI] 3.24303e-05
OSMED [NCBI] 3.24303e-05
PTGS1 [NCBI] 3.10437e-05
GGCX [NCBI] 3.10437e-05
MTC [NCBI] 3.10355e-05
wildervanck syndrome [NCBI] 3.10355e-05
severe cutaneous adverse reaction, susceptibility to [NCBI] 3.10355e-05
PCNA [NCBI] 3.02094e-05
NLRP3 [NCBI] 3.01543e-05
SGD [NCBI] 2.97639e-05
SEDT [NCBI] 2.97639e-05
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 2.97639e-05
IKBKB [NCBI] 2.93406e-05
TCRB [NCBI] 2.93406e-05
KLK7 [NCBI] 2.93406e-05
ALUNC [NCBI] 2.85967e-05
PRKCM [NCBI] 2.85907e-05
APC [NCBI] 2.75267e-05
ichthyosis vulgaris [NCBI] 2.75187e-05
HR [NCBI] 2.7248e-05
KRT1 [NCBI] 2.66418e-05
kawasaki disease [NCBI] 2.65181e-05
muckle-wells syndrome [NCBI] 2.65181e-05
GVM [NCBI] 2.65181e-05
severe combined immunodeficiency with sensitivity to ionizing radiation [NCBI] 2.65181e-05
XPD [NCBI] 2.65181e-05
tyrosine transaminase deficiency [NCBI] 2.60723e-05
lymphoma, non-hodgkin, familial [NCBI] 2.56956e-05
CGD [NCBI] 2.56442e-05
EPPK [NCBI] 2.55852e-05
synovitis, granulomatous, with uveitis and cranial neuropathies [NCBI] 2.55852e-05
C4B [NCBI] 2.55353e-05
ECM1 [NCBI] 2.55353e-05
GJB6 [NCBI] 2.50274e-05
DKC1 [NCBI] 2.50274e-05
CYLD [NCBI] 2.47119e-05
amyloidosis v [NCBI] 2.47119e-05
erythermalgia, primary [NCBI] 2.47119e-05
ED2 [NCBI] 2.47119e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 2.47119e-05
TNFSF8 [NCBI] 2.45458e-05
HLA-B [NCBI] 2.45458e-05
CDPX1 [NCBI] 2.38918e-05
holocarboxylase synthetase deficiency [NCBI] 2.38918e-05
hartnup disorder [NCBI] 2.31191e-05
cutis laxa, autosomal recessive, type i [NCBI] 2.23892e-05
AGS1 [NCBI] 2.23892e-05
ERCC2 [NCBI] 2.20868e-05
XPC [NCBI] 2.20868e-05
mucolipidosis iiia [NCBI] 2.16979e-05
KLF4 [NCBI] 2.10672e-05
AFD1 [NCBI] 2.10417e-05
MNS [NCBI] 2.10417e-05
TRPS1 [NCBI] 2.10417e-05
AHO [NCBI] 2.09093e-05
aspartylglucosaminuria [NCBI] 2.07514e-05
HIDS [NCBI] 2.04176e-05
APL [NCBI] 2.04176e-05
ehlers-danlos syndrome, type vi [NCBI] 1.98228e-05
C3 [NCBI] 1.95885e-05
GLA [NCBI] 1.932e-05
ALK [NCBI] 1.91166e-05
DSG1 [NCBI] 1.90594e-05
LOX [NCBI] 1.90594e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 1.87124e-05
CD [NCBI] 1.86952e-05
PTH [NCBI] 1.86609e-05
OA1 [NCBI] 1.85602e-05
FGF7 [NCBI] 1.82816e-05
OFD1 [NCBI] 1.81928e-05
biotinidase deficiency [NCBI] 1.81928e-05
FGFR3 [NCBI] 1.79183e-05
RBP1 [NCBI] 1.7861e-05
epidermolysis bullosa letalis [NCBI] 1.76947e-05
EBR1 [NCBI] 1.72165e-05
COL7A1 [NCBI] 1.72138e-05
RNASE3 [NCBI] 1.71458e-05
MC1R [NCBI] 1.70085e-05
leopard syndrome 1 [NCBI] 1.6757e-05
TPMT [NCBI] 1.6612e-05
LCN2 [NCBI] 1.64204e-05
FMF [NCBI] 1.62639e-05
FGF23 [NCBI] 1.62331e-05
MSH2 [NCBI] 1.60498e-05
OCRL [NCBI] 1.54787e-05
FPLD2 [NCBI] 1.54787e-05
FCAS [NCBI] 1.47005e-05
UCN [NCBI] 1.45596e-05
CDPX2 [NCBI] 1.43311e-05
apert syndrome [NCBI] 1.43311e-05
ehlers-danlos syndrome, type i [NCBI] 1.39738e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 1.38353e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 1.36281e-05
CNC1 [NCBI] 1.32934e-05
MPO [NCBI] 1.29273e-05
MLH1 [NCBI] 1.27975e-05
POMC [NCBI] 1.24221e-05
XPA [NCBI] 1.17658e-05
BCPM [NCBI] 1.1215e-05
CTGF [NCBI] 1.11681e-05
MPZ [NCBI] 1.10643e-05
neuraminidase deficiency [NCBI] 9.73321e-06
costello syndrome [NCBI] 9.50827e-06
CEACAM5 [NCBI] 9.0302e-06
sickle cell anemia [NCBI] 8.86664e-06
RET [NCBI] 8.23206e-06
HMBS [NCBI] 8.23206e-06
porphyria, acute intermittent [NCBI] 8.08155e-06
AR [NCBI] 7.86811e-06
temporal arteritis [NCBI] 7.81692e-06
PTEN [NCBI] 7.61979e-06
FGFR2 [NCBI] 7.61979e-06
APRT [NCBI] 7.56173e-06
CRMO [NCBI] 7.3675e-06
SDC2 [NCBI] 6.80238e-06
apc gene [NCBI] 6.75168e-06
ALGS1 [NCBI] 6.56194e-06
CVID [NCBI] 6.48059e-06
OCP [NCBI] 5.84053e-06
MBP [NCBI] 5.76125e-06
HGPS [NCBI] 5.70534e-06
BLM [NCBI] 5.70534e-06
NPY [NCBI] 5.56387e-06
FOP [NCBI] 5.44343e-06
CRH [NCBI] 5.39246e-06
HGF [NCBI] 5.25745e-06
PSORS1 [NCBI] 4.95148e-06
TTR [NCBI] 4.82379e-06
DFSP [NCBI] 3.93647e-06
EGF [NCBI] 3.62522e-06
ACHE [NCBI] 3.1867e-06
TH [NCBI] 3.13898e-06
hypercholesterolemia, autosomal dominant [NCBI] 3.01347e-06
EGFR [NCBI] 2.57839e-06
AT [NCBI] 2.41373e-06
MUC1 [NCBI] 2.39213e-06
IL2 [NCBI] 2.35904e-06
HP [NCBI] 1.99726e-06
MAS [NCBI] 1.77076e-06
GAPDH [NCBI] 1.76659e-06
ADA [NCBI] 1.75466e-06
WAS [NCBI] 1.69128e-06
PF4 [NCBI] 1.4526e-06
VHL [NCBI] 1.37681e-06
G6PD [NCBI] 1.19461e-06
VIP [NCBI] 7.81442e-07
TNF [NCBI] 7.42068e-07
KSS [NCBI] 5.45482e-07
HPS [NCBI] 5.20563e-07
PTK2 [NCBI] 4.44925e-07
TYMS [NCBI] 3.4985e-07
dystrophia myotonica 1 [NCBI] 2.17939e-07
BCNS [NCBI] 1.95583e-07
CAT [NCBI] 1.02038e-07
SLOS [NCBI] 8.04133e-08
APOB [NCBI] 6.83012e-08
LAM [NCBI] 3.8456e-08
SLE [NCBI] 2.66443e-08
APOE [NCBI] 7.35177e-09
SPP1 [NCBI] 5.85502e-09
CHAT [NCBI] 2.55016e-10




Database Center for Life Science