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01 Nail Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
NDIC [NCBI] 0.000438875
TYS [NCBI] 0.000438875
KRT17 [NCBI] 8.68519e-05
GJB6 [NCBI] 1.92736e-05
KRT85 [NCBI] 1.77972e-05
C7orf11 [NCBI] 1.39349e-05
RSPO4 [NCBI] 1.31553e-05
NSDHL [NCBI] 1.16119e-05
KRT6B [NCBI] 1.16119e-05
KRT6A [NCBI] 1.10709e-05
KRT16 [NCBI] 1.08947e-05
FOXN1 [NCBI] 1.08129e-05
CD34 [NCBI] 9.21733e-06
COL7A1 [NCBI] 8.63622e-06
DKC1 [NCBI] 8.54891e-06
TGM1 [NCBI] 8.06967e-06
DSG1 [NCBI] 7.74838e-06
TYRP1 [NCBI] 7.6451e-06
ERCC5 [NCBI] 7.52422e-06
HLA-C [NCBI] 6.77276e-06
DSG3 [NCBI] 6.76528e-06
OSM [NCBI] 6.31011e-06
CD99 [NCBI] 6.29875e-06
ERCC1 [NCBI] 6.25406e-06
PRKDC [NCBI] 5.96595e-06
ERCC2 [NCBI] 5.84933e-06
GJB1 [NCBI] 5.81502e-06
G6PD [NCBI] 4.49881e-06
PCNA [NCBI] 2.65721e-06
PTH [NCBI] 2.05926e-06
EGFR [NCBI] 2.04198e-06



OMIM


 OMIM Link Information
gain		 01
leukonychia totalis [NCBI] 0.0027714
DKC [NCBI] 0.000862676
anonychia-onychodystrophy with hypoplasia or absence of distal phalanges [NCBI] 0.000817902
trichorrhexis nodosa syndrome [NCBI] 0.000693453
sclerotylosis [NCBI] 0.000667246
schopf-schulz-passarge syndrome [NCBI] 0.000644828
PC1 [NCBI] 0.000577065
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000553054
KRT17 [NCBI] 0.000367641
pachyonychia congenita, recessive [NCBI] 0.000211707
PURE&apos [NCBI] 0.00018813
steatocystoma multiplex [NCBI] 0.000180779
DPR [NCBI] 0.000180779
KRT6B [NCBI] 0.000177768
PC2 [NCBI] 0.000165434
KRT6A [NCBI] 0.000150209
nail dysplasia, isolated congenital [NCBI] 0.000150209
TTDP [NCBI] 0.000137418
odontomicronychial dysplasia [NCBI] 0.000121164
t-cell immunodeficiency, congenital alopecia, and nail dystrophy [NCBI] 9.87009e-05
steatocystoma multiplex with natal teeth [NCBI] 9.02278e-05
KRTHB5 [NCBI] 8.86222e-05
keratin 6, hair follicle [NCBI] 8.86222e-05
LOCS [NCBI] 8.47286e-05
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 8.47286e-05
yellow nail syndrome [NCBI] 8.06418e-05
epidermolysis bullosa pruriginosa [NCBI] 7.73868e-05
IP [NCBI] 7.46367e-05
HMS [NCBI] 7.23669e-05
psoriatic arthritis, susceptibility to [NCBI] 7.23669e-05
FOXN1 [NCBI] 6.96426e-05
dyskeratosis congenita, autosomal dominant [NCBI] 6.85485e-05
TTDN1 [NCBI] 6.17553e-05
KRT16 [NCBI] 6.00921e-05
epidermolysis bullosa simplex and limb-girdle muscular dystrophy [NCBI] 5.96579e-05
GJB6 [NCBI] 4.91793e-05
DKC1 [NCBI] 4.91793e-05
TGM1 [NCBI] 4.86833e-05
KRT14 [NCBI] 4.65199e-05
LI1 [NCBI] 4.18322e-05
PSORS1 [NCBI] 3.43558e-05
APS1 [NCBI] 3.06825e-05
RA [NCBI] 2.31755e-05
LAM [NCBI] 2.18941e-05
CVID [NCBI] 1.3466e-05
G6PD [NCBI] 1.13232e-05
TS [NCBI] 8.09421e-06
PCNA [NCBI] 3.83875e-06
EGFR [NCBI] 2.38406e-06
SLE [NCBI] 2.04229e-06
PTH [NCBI] 1.68736e-06



Database Center for Life Science