Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Nails [NCBI]

Gene


 Gene Link Information
Gain		 01
APEX1 [NCBI] 1.1952e-05
GSTT1 [NCBI] 1.18126e-05
GSTM1 [NCBI] 1.10933e-05
XPA [NCBI] 1.10667e-05
TGM1 [NCBI] 1.10667e-05
TYRP1 [NCBI] 1.05864e-05
TCHH [NCBI] 8.33999e-06
DNASE1L2 [NCBI] 7.70175e-06
SCEL [NCBI] 7.59028e-06
LMX1B [NCBI] 7.16669e-06
KRT17 [NCBI] 6.81997e-06
IRF6 [NCBI] 6.42228e-06
GJB6 [NCBI] 5.77062e-06
OGG1 [NCBI] 5.59831e-06
FOXN1 [NCBI] 5.50235e-06
NAGA [NCBI] 5.47655e-06
ERCC4 [NCBI] 5.43905e-06
HLA-DQA1 [NCBI] 5.36803e-06
ERCC5 [NCBI] 5.36803e-06
KRT10 [NCBI] 5.33434e-06
KRT5 [NCBI] 5.28059e-06
XRCC1 [NCBI] 5.23958e-06
ERCC1 [NCBI] 4.70753e-06
ERCC2 [NCBI] 4.68425e-06
PIH [NCBI] 4.63379e-06
KRT20 [NCBI] 4.2053e-06
CYP2C19 [NCBI] 4.1568e-06
DCT [NCBI] 4.05109e-06
GSTP1 [NCBI] 3.94736e-06
IL6 [NCBI] 3.04944e-06
VWF [NCBI] 2.33738e-06
PCNA [NCBI] 1.98025e-06
EGFR [NCBI] 1.73767e-06
TNF [NCBI] 8.54352e-07



OMIM


 OMIM Link Information
gain		 01
nail dysplasia [NCBI] 0.00300245
ameloonychohypohidrotic syndrome [NCBI] 0.00148718
leukonychia totalis [NCBI] 0.00148718
zinc, elevated plasma [NCBI] 0.00117647
epidermolysis bullosa inversa dystrophica [NCBI] 0.00105937
onychotrichodysplasia and neutropenia [NCBI] 0.000983418
trichorrhexis nodosa syndrome [NCBI] 0.000882123
behcet syndrome [NCBI] 0.000638468
polyposis, skin pigmentation, alopecia, and fingernail changes [NCBI] 0.000322665
SLE [NCBI] 0.000305273
DKC [NCBI] 0.000303121
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 0.000298249
pachyonychia congenita, recessive [NCBI] 0.000188151
nail high-sulfur protein [NCBI] 0.000188151
endothelial dystrophy, congenital hereditary, with nail hypoplasia [NCBI] 0.000188151
ectodermal dysplasia, hidrotic, christianson-fourie type [NCBI] 0.000188151
KRN1 [NCBI] 0.000177704
LI1 [NCBI] 0.000160724
t-cell immunodeficiency, congenital alopecia, and nail dystrophy [NCBI] 0.000148911
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies [NCBI] 0.000148911
curved nail of fourth toe [NCBI] 0.000148911
steatocystoma multiplex with natal teeth [NCBI] 0.000148911
NPS [NCBI] 0.00014774
epidermolysis bullosa with congenital localized absence of skin and deformity of nails [NCBI] 0.000134122
yellow nail syndrome [NCBI] 0.000134122
witkop syndrome [NCBI] 0.000124532
PURE&apos [NCBI] 0.000124532
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 0.000124532
anonychia congenita [NCBI] 0.00011741
nail dysplasia, isolated congenital [NCBI] 0.000114243
TTDN1 [NCBI] 0.000111742
epidermolysis bullosa herpetiformis, dowling-meara type [NCBI] 0.000111742
FOXN1 [NCBI] 0.000101814
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 9.94954e-05
ED2 [NCBI] 8.87068e-05
TTDP [NCBI] 8.45733e-05
TGM1 [NCBI] 8.34447e-05
epidermolysis bullosa letalis [NCBI] 8.27198e-05
AFD1 [NCBI] 7.78157e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 7.24157e-05
BCPM [NCBI] 6.40897e-05
VWS [NCBI] 5.51302e-05
APS1 [NCBI] 5.3308e-05
KRTHA6 [NCBI] 5.31535e-05
HHT [NCBI] 5.05378e-05
wilson disease [NCBI] 4.75776e-05
KRT17 [NCBI] 4.62333e-05
KRT10 [NCBI] 4.34985e-05
GJB6 [NCBI] 3.9525e-05
COL7A1 [NCBI] 3.58526e-05
IP [NCBI] 3.23949e-05
CF [NCBI] 2.86245e-05
PXE [NCBI] 2.486e-05
RA [NCBI] 2.20159e-05
FMF [NCBI] 1.77456e-05
MUC1 [NCBI] 1.61129e-05
CEACAM5 [NCBI] 6.63864e-06
VEGF [NCBI] 5.41385e-06
PCNA [NCBI] 4.70908e-06
EGFR [NCBI] 4.25752e-06
RP [NCBI] 3.682e-06



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