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MeSH keywords -> Related genes, diseases (OMIM)


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01 Nails, Malformed [NCBI]


Gene


Gene Link Information
Gain
01
NDIC [NCBI] 0.000438875
ZLS [NCBI] 0.000340315
RSPO4 [NCBI] 6.37835e-05
KRT16 [NCBI] 3.78812e-05
COL7A1 [NCBI] 3.09061e-05
DLX3 [NCBI] 2.05024e-05
KRT71 [NCBI] 1.75004e-05
KRTAP17-1 [NCBI] 1.75004e-05
IKBKE [NCBI] 1.44662e-05
CHUK [NCBI] 1.41168e-05
IKBKB [NCBI] 1.40961e-05
WNT10A [NCBI] 1.32042e-05
WNT6 [NCBI] 1.28585e-05
VIL1 [NCBI] 1.28585e-05
DNAJB2 [NCBI] 1.25711e-05
EN1 [NCBI] 1.2325e-05
EPHA4 [NCBI] 1.14473e-05
EVC [NCBI] 1.1078e-05
KRT6A [NCBI] 1.07742e-05
KRT17 [NCBI] 1.06839e-05
FOXN1 [NCBI] 1.05163e-05
HAND2 [NCBI] 1.04383e-05
LMX1B [NCBI] 1.04383e-05
ROR2 [NCBI] 1.02922e-05
EDAR [NCBI] 1.02922e-05
WNT7A [NCBI] 1.01575e-05
MSX1 [NCBI] 9.26852e-06
INHA [NCBI] 8.92106e-06
KRT5 [NCBI] 7.50691e-06
RUNX2 [NCBI] 7.47967e-06
LMNA [NCBI] 6.26085e-06
SHH [NCBI] 5.83325e-06
ERCC2 [NCBI] 5.5565e-06
TP63 [NCBI] 5.39198e-06
VHL [NCBI] 4.56513e-06




OMIM


OMIM Link Information
gain
01
deafness, congenital, and onychodystrophy, recessive form [NCBI] 0.00782442
coffin-siris syndrome [NCBI] 0.00689527
onychotrichodysplasia and neutropenia [NCBI] 0.00205655
ZLS [NCBI] 0.00135668
anonychia-onychodystrophy with hypoplasia or absence of distal phalanges [NCBI] 0.00130408
ectodermal dysplasia, absent dermatoglyphic pattern, changes in nails, and simian crease [NCBI] 0.00130408
koilonychia, hereditary [NCBI] 0.00116933
leukonychia totalis [NCBI] 0.00100669
schopf-schulz-passarge syndrome [NCBI] 0.00090173
brachydactyly, type a5, with nail dysplasia [NCBI] 0.000800285
coloboma of macula [NCBI] 0.000800285
triphalangeal thumb, nonopposable [NCBI] 0.000800285
curly hair-acral keratoderma-caries syndrome [NCBI] 0.000800285
PC1 [NCBI] 0.000693866
anonychia congenita [NCBI] 0.000589259
otoonychoperoneal syndrome [NCBI] 0.000583287
nail dysplasia [NCBI] 0.000583287
NPS [NCBI] 0.000523618
symphalangism, distal [NCBI] 0.000501982
dermal ridges, patternless [NCBI] 0.000501982
sabinas brittle hair syndrome [NCBI] 0.000501982
FRNS [NCBI] 0.0004746
DKC [NCBI] 0.00044224
PC2 [NCBI] 0.000429364
AOS [NCBI] 0.000383886
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.000380062
witkop syndrome [NCBI] 0.000361483
hypertelorism, teebi type [NCBI] 0.000354699
sclerotylosis [NCBI] 0.000354699
epidermolysis bullosa with congenital localized absence of skin and deformity of nails [NCBI] 0.000345923
arthrogryposis and ectodermal dysplasia [NCBI] 0.000317322
RA [NCBI] 0.000299009
OODD [NCBI] 0.000280882
PURE&apos [NCBI] 0.000262819
RSPO4 [NCBI] 0.000259075
nail dysplasia, isolated congenital [NCBI] 0.000236716
COL7A1 [NCBI] 0.000212154
KRT16 [NCBI] 0.000211561
ectodermal dysplasia, trichoodontoonychial type [NCBI] 0.000211424
curved nail of fourth toe [NCBI] 0.000211424
tonoki syndrome [NCBI] 0.000211424
SLE [NCBI] 0.000211297
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000194362
KRT17 [NCBI] 0.000192009
ROR2 [NCBI] 0.00018234
brachymorphism-onychodysplasia-dysphalangism syndrome [NCBI] 0.000180493
hearing loss, sensorineural, with enamel hypoplasia and nail defects [NCBI] 0.000166526
yellow nail syndrome [NCBI] 0.000156945
weyers acrofacial dysostosis [NCBI] 0.000149609
steatocystoma multiplex [NCBI] 0.000149609
FDH [NCBI] 0.000139639
monilethrix [NCBI] 0.000130495
anonychia-ectrodactyly [NCBI] 0.00010565
anonychia-onychodystrophy [NCBI] 0.00010565
trichoodontoonychial dysplasia [NCBI] 0.00010565
anonychia, total, with microcephaly [NCBI] 0.00010565
endothelial dystrophy, congenital hereditary, with nail hypoplasia [NCBI] 0.00010565
anonychia-onychodystrophy with brachydactyly type b and ectrodactyly [NCBI] 0.00010565
ectodermal dysplasia with adrenal cyst [NCBI] 0.00010565
hirschsprung disease with hypoplastic nails and dysmorphic facial features [NCBI] 0.00010565
corneodermatoosseous syndrome [NCBI] 0.00010565
odontotrichoungual-digital-palmar syndrome [NCBI] 0.00010565
anonychia with flexural pigmentation [NCBI] 0.00010565
ulnar hypoplasia with mental retardation [NCBI] 0.00010565
ectodermal dysplasia, hidrotic, christianson-fourie type [NCBI] 0.00010565
hirschsprung disease with type d brachydactyly [NCBI] 0.00010565
sella turcica, bridged [NCBI] 0.00010565
onycholysis, partial, with scleronychia [NCBI] 0.00010565
CFNS [NCBI] 9.29736e-05
WNT10A [NCBI] 8.5955e-05
KRN1 [NCBI] 8.5955e-05
trigonocephaly with short stature and developmental delay [NCBI] 8.32014e-05
dermoodontodysplasia [NCBI] 8.32014e-05
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities [NCBI] 8.32014e-05
pachyonychia congenita, recessive [NCBI] 7.47431e-05
chands [NCBI] 7.47431e-05
toenail dystrophy, isolated [NCBI] 7.47431e-05
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy [NCBI] 7.47431e-05
LOCS [NCBI] 6.92586e-05
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 6.92586e-05
coloboma of macula with type b brachydactyly [NCBI] 6.92586e-05
carbimazole sensitivity [NCBI] 6.92586e-05
dyskeratosis congenita, autosomal recessive [NCBI] 6.92586e-05
polyposis, skin pigmentation, alopecia, and fingernail changes [NCBI] 6.92586e-05
kabuki syndrome [NCBI] 6.85218e-05
FOXN1 [NCBI] 6.69762e-05
ED3 [NCBI] 6.51865e-05
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 6.51865e-05
scalp-ear-nipple syndrome [NCBI] 6.51865e-05
KRT6A [NCBI] 6.36001e-05
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [NCBI] 6.19463e-05
frontonasal dysplasia [NCBI] 5.69559e-05
BDB1 [NCBI] 5.31672e-05
lymphedema, hereditary, ii [NCBI] 5.31672e-05
KRT10 [NCBI] 5.26608e-05
adult syndrome [NCBI] 4.87868e-05
SYNS1 [NCBI] 4.87868e-05
lymphedema, hereditary, i [NCBI] 4.87868e-05
MSX1 [NCBI] 4.81758e-05
indifference to pain, congenital, autosomal recessive [NCBI] 4.75625e-05
LMS [NCBI] 4.64275e-05
IP [NCBI] 4.54029e-05
epidermolysis bullosa simplex and limb-girdle muscular dystrophy [NCBI] 4.438e-05
DRRS [NCBI] 4.34497e-05
ED2 [NCBI] 4.34497e-05
COL17A1 [NCBI] 4.20915e-05
RHS [NCBI] 4.09559e-05
robinow syndrome, autosomal recessive [NCBI] 4.02075e-05
GABEB [NCBI] 3.94943e-05
weaver syndrome [NCBI] 3.88132e-05
PPS [NCBI] 3.81614e-05
HMI [NCBI] 3.81408e-05
epidermolysis bullosa letalis [NCBI] 3.58051e-05
leopard syndrome 1 [NCBI] 3.47533e-05
CDPX2 [NCBI] 3.19853e-05
charge syndrome [NCBI] 3.1571e-05
EVC [NCBI] 3.11682e-05
exostoses, multiple, type i [NCBI] 3.07764e-05
cardiofaciocutaneous syndrome [NCBI] 3.0395e-05
PHS [NCBI] 2.93082e-05
CMTC [NCBI] 2.86273e-05
HGPS [NCBI] 2.11346e-05
AHO [NCBI] 1.72336e-05
WBS [NCBI] 8.40602e-06




Database Center for Life Science