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01 Ectodermal Dysplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
EDA [NCBI] 0.00075169
EEC2 [NCBI] 0.000438875
EEC1 [NCBI] 0.000438875
TP63 [NCBI] 0.000305403
EDAR [NCBI] 0.000264891
IKBKG [NCBI] 0.000193585
IKBKE [NCBI] 0.000140979
CHUK [NCBI] 0.000128312
IKBKB [NCBI] 0.000128132
PKP1 [NCBI] 0.000127639
CKAP4 [NCBI] 9.53709e-05
EDARADD [NCBI] 9.16573e-05
GJB6 [NCBI] 8.92891e-05
TRAF6 [NCBI] 5.94107e-05
KRT17 [NCBI] 5.19687e-05
KRT16 [NCBI] 5.14889e-05
DLX3 [NCBI] 4.30291e-05
EDA2R [NCBI] 3.69627e-05
PVRL1 [NCBI] 2.85167e-05
HNRNPAB [NCBI] 2.19289e-05
TRAF5 [NCBI] 1.98959e-05
MAP3K7IP2 [NCBI] 1.89061e-05
MAP3K14 [NCBI] 1.86572e-05
MAP2K2 [NCBI] 1.86572e-05
KRT14 [NCBI] 1.75161e-05
MAP3K7 [NCBI] 1.73285e-05
TRAF3 [NCBI] 1.56513e-05
TRAF2 [NCBI] 1.56513e-05
KRT71 [NCBI] 1.42385e-05
FOXI3 [NCBI] 1.42385e-05
KRT85 [NCBI] 1.42385e-05
KRT24 [NCBI] 1.42385e-05
NFKBIA [NCBI] 1.34527e-05
AIRE [NCBI] 1.17614e-05
NFKBIB [NCBI] 1.14287e-05
SFRS15 [NCBI] 1.09604e-05
TNFRSF19 [NCBI] 1.09604e-05
C7orf11 [NCBI] 1.03773e-05
GJB2 [NCBI] 1.01841e-05
WNT10A [NCBI] 9.94388e-06
BRAF [NCBI] 9.71147e-06
WNT6 [NCBI] 9.59854e-06
VIL1 [NCBI] 9.59854e-06
DNAJB2 [NCBI] 9.31144e-06
KLK9 [NCBI] 9.31144e-06
TUBA3C [NCBI] 8.85094e-06
RPLP0 [NCBI] 8.66017e-06
EPHA4 [NCBI] 8.18987e-06
MAP2K1 [NCBI] 8.05986e-06
KRT6A [NCBI] 7.519e-06
TRAF1 [NCBI] 7.42901e-06
ALX4 [NCBI] 7.42901e-06
NCF1 [NCBI] 7.11026e-06
REL [NCBI] 6.72233e-06
GNB2L1 [NCBI] 6.72233e-06
ABCD3 [NCBI] 6.61053e-06
FURIN [NCBI] 6.55729e-06
IRAK4 [NCBI] 6.40695e-06
LTB [NCBI] 6.40695e-06
ACTB [NCBI] 6.35968e-06
NFKB1 [NCBI] 6.34701e-06
CDH3 [NCBI] 6.31369e-06
INHA [NCBI] 5.67898e-06
LEF1 [NCBI] 5.58825e-06
GJB3 [NCBI] 5.42039e-06
ITGB4 [NCBI] 5.34241e-06
INHBA [NCBI] 4.99957e-06
GJA1 [NCBI] 4.68154e-06
FGF4 [NCBI] 4.58257e-06
SFN [NCBI] 4.37269e-06
KRT5 [NCBI] 4.29045e-06
CD40 [NCBI] 4.18694e-06
FGFR2 [NCBI] 3.57132e-06
CYBB [NCBI] 3.06878e-06
GAPDH [NCBI] 2.61012e-06
TNF [NCBI] 2.52503e-06
ERCC2 [NCBI] 2.43777e-06
GJB1 [NCBI] 2.40647e-06
CTNNB1 [NCBI] 2.30744e-06
KRAS [NCBI] 2.22206e-06
G6PD [NCBI] 1.2683e-06
CDKN1A [NCBI] 9.24572e-07
HRAS [NCBI] 9.1602e-07
EGF [NCBI] 5.2734e-07



OMIM


 OMIM Link Information
gain		 01
EEC1 [NCBI] 0.0162231
schopf-schulz-passarge syndrome [NCBI] 0.00483984
ED1 [NCBI] 0.0041661
AOS [NCBI] 0.00349495
ACC [NCBI] 0.00282528
facial ectodermal dysplasia [NCBI] 0.00236053
cranioectodermal dysplasia [NCBI] 0.00215615
focal facial dermal dysplasia [NCBI] 0.00191171
RHS [NCBI] 0.00169584
lelis syndrome [NCBI] 0.00150732
ED2 [NCBI] 0.00141493
ectodermal dysplasia, absent dermatoglyphic pattern, changes in nails, and simian crease [NCBI] 0.00120839
EDA [NCBI] 0.00111103
EEC3 [NCBI] 0.00108085
rosselli-gulienetti syndrome [NCBI] 0.00107399
trichorrhexis nodosa syndrome [NCBI] 0.000912034
dermatoglyphics--fingerprint pattern [NCBI] 0.000752637
ameloonychohypohidrotic syndrome [NCBI] 0.000752637
LMS [NCBI] 0.000687749
ectodermal dysplasia, anhidrotic [NCBI] 0.000566853
IKBKG [NCBI] 0.000566758
ankyloblepharon-ectodermal defects-cleft lip/palate [NCBI] 0.00054485
CLPED1 [NCBI] 0.00054485
otodental dysplasia [NCBI] 0.000535985
fingerprints, absence of [NCBI] 0.000535985
adult syndrome [NCBI] 0.000516379
TP73L [NCBI] 0.00051422
PURE&apos [NCBI] 0.000472222
uncombable hair syndrome [NCBI] 0.000455025
sabinas brittle hair syndrome [NCBI] 0.000455025
EDAR [NCBI] 0.000449826
woolly hair, autosomal dominant [NCBI] 0.000402908
ectodermal dysplasia, hypohidrotic, with immune deficiency [NCBI] 0.00038657
OODD [NCBI] 0.000377655
PC2 [NCBI] 0.000372188
distichiasis [NCBI] 0.00036449
ED3 [NCBI] 0.000337143
PPPP [NCBI] 0.000334141
keratosis palmoplantaris papulosa [NCBI] 0.000334141
SHFM1 [NCBI] 0.000321976
ectodermal dysplasia/skin fragility syndrome [NCBI] 0.00031584
aplasia cutis congenita with epibulbar dermoids [NCBI] 0.00031584
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.000309123
SHFM2 [NCBI] 0.000309123
naegeli syndrome [NCBI] 0.000300305
KRT17 [NCBI] 0.000293545
popliteal pterygium syndrome, lethal type [NCBI] 0.000287894
blepharocheilodontic syndrome [NCBI] 0.000287894
cerebellar ataxia and ectodermal dysplasia [NCBI] 0.000283149
arthrogryposis and ectodermal dysplasia [NCBI] 0.000283149
EDARADD [NCBI] 0.000274499
JBS [NCBI] 0.000274029
AKE [NCBI] 0.000269498
GJB6 [NCBI] 0.000262806
KRT16 [NCBI] 0.000251861
eem syndrome [NCBI] 0.000246733
witkop syndrome [NCBI] 0.000215874
DPR [NCBI] 0.000215874
deafness, congenital, and onychodystrophy, recessive form [NCBI] 0.000203253
PKP1 [NCBI] 0.000201977
TOC [NCBI] 0.000193323
aredyld [NCBI] 0.000188704
dermoodontodysplasia [NCBI] 0.000188704
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia [NCBI] 0.000188704
ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [NCBI] 0.000188704
tetra-amelia with ectodermal dysplasia and lacrimal duct abnormalities [NCBI] 0.000188704
ectodermal dysplasia, trichoodontoonychial type [NCBI] 0.000188704
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities [NCBI] 0.000188704
KRT14 [NCBI] 0.000188518
SHFM3 [NCBI] 0.000167677
FDH [NCBI] 0.000160794
marshall syndrome [NCBI] 0.000158604
alopecia-contractures-dwarfism mental retardation syndrome [NCBI] 0.000157798
chands [NCBI] 0.000157798
steatocystoma multiplex with natal teeth [NCBI] 0.000157798
immunodeficiency without anhidrotic ectodermal dysplasia [NCBI] 0.000157798
ectodysplasin receptor, x-linked [NCBI] 0.000149428
taurodontism [NCBI] 0.000143855
scalp-ear-nipple syndrome [NCBI] 0.000134299
IP [NCBI] 0.000130603
steatocystoma multiplex [NCBI] 0.000126987
DKC [NCBI] 0.000112187
cardiofaciocutaneous syndrome [NCBI] 0.000110987
APS1 [NCBI] 0.000107577
PVRL1 [NCBI] 0.000102074
PC1 [NCBI] 9.62049e-05
ectodermal dysplasia with natal teeth, turnpenny type [NCBI] 9.43216e-05
ectodermal dysplasia, hidrotic, autosomal recessive [NCBI] 9.43216e-05
arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay [NCBI] 9.43216e-05
OTD [NCBI] 9.43216e-05
pilodental dysplasia with refractive errors [NCBI] 9.43216e-05
anhidrosis [NCBI] 9.43216e-05
thumb deformity and alopecia [NCBI] 9.43216e-05
charcot-marie-tooth peroneal muscular atrophy, x-linked, with aplasia cutis congenita [NCBI] 9.43216e-05
ectodermal dysplasia with adrenal cyst [NCBI] 9.43216e-05
ectodermal dysplasia and neurosensory deafness [NCBI] 9.43216e-05
amelia, autosomal recessive [NCBI] 9.43216e-05
brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia [NCBI] 9.43216e-05
ACCCA [NCBI] 9.43216e-05
CASS [NCBI] 9.43216e-05
odontotrichoungual-digital-palmar syndrome [NCBI] 9.43216e-05
ectodermal dysplasia with mental retardation and syndactyly [NCBI] 9.43216e-05
gonadal dysgenesis, xy type, with associated anomalies [NCBI] 9.43216e-05
ectodermal dysplasia, hidrotic, christianson-fourie type [NCBI] 9.43216e-05
ASDP [NCBI] 9.43216e-05
hyperpigmentation of fuldauer and kuijpers [NCBI] 9.43216e-05
OLEDAID [NCBI] 9.43216e-05
teeth, congenital absence of, with taurodontia and sparse hair [NCBI] 9.43216e-05
dermatoosteolysis, kirghizian type [NCBI] 9.43216e-05
trichoodontoonychial dysplasia [NCBI] 9.43216e-05
incisors, lower central, absence of [NCBI] 9.43216e-05
trichodysplasia-xeroderma [NCBI] 9.43216e-05
ackerman syndrome [NCBI] 9.43216e-05
ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet [NCBI] 9.43216e-05
rodrigues blindness [NCBI] 9.43216e-05
NETH [NCBI] 8.76861e-05
SMMCI [NCBI] 8.58789e-05
TTDP [NCBI] 8.41722e-05
ATD1 [NCBI] 8.00579e-05
WNT10A [NCBI] 7.46511e-05
TNFRSF19 [NCBI] 7.46511e-05
KRT24 [NCBI] 7.46511e-05
KRTHB5 [NCBI] 7.46511e-05
epidermolysis bullosa with pyloric atresia [NCBI] 7.4332e-05
ectrodactyly and ectodermal dysplasia without cleft lip/palate [NCBI] 7.18971e-05
aplasia cutis congenita, high myopia, and cone-rod dysfunction [NCBI] 7.18971e-05
sener syndrome [NCBI] 7.18971e-05
trichodental dysplasia [NCBI] 7.18971e-05
uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly [NCBI] 7.18971e-05
pena-shokeir syndrome, type i [NCBI] 6.85227e-05
LTB [NCBI] 6.08757e-05
DOCK8 [NCBI] 6.08757e-05
carbimazole sensitivity [NCBI] 5.80029e-05
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [NCBI] 5.80029e-05
FOXN1 [NCBI] 5.56797e-05
barber-say syndrome [NCBI] 5.39551e-05
progeroid short stature with pigmented nevi [NCBI] 5.39551e-05
KRT6A [NCBI] 5.23073e-05
cerebellotrigeminal dermal dysplasia [NCBI] 5.07392e-05
SHFM4 [NCBI] 5.07392e-05
zunich neuroectodermal syndrome [NCBI] 5.07392e-05
ENO1 [NCBI] 4.98009e-05
NFKB2 [NCBI] 4.98009e-05
achondroplasia, so-called, and severe combined immunodeficiency [NCBI] 4.80729e-05
TTDN1 [NCBI] 4.80729e-05
NFKBIA [NCBI] 4.78047e-05
TTDN1 [NCBI] 4.78047e-05
CDH3 [NCBI] 4.78047e-05
keratoderma, palmoplantar, with deafness [NCBI] 4.57973e-05
ALDOA [NCBI] 4.4726e-05
naxos disease [NCBI] 4.38139e-05
TRAF6 [NCBI] 4.34856e-05
RELA [NCBI] 4.23842e-05
MSX2 [NCBI] 4.13939e-05
KRT10 [NCBI] 4.13939e-05
oculocerebrocutaneous syndrome [NCBI] 3.9054e-05
chromosome 18q deletion syndrome [NCBI] 3.9054e-05
COL11A1 [NCBI] 3.89104e-05
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 3.77497e-05
ALUNC [NCBI] 3.65496e-05
PFM [NCBI] 3.54389e-05
multiple pterygium syndrome, escobar variant [NCBI] 3.54389e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 3.2534e-05
omenn syndrome [NCBI] 3.16811e-05
NFKB1 [NCBI] 3.05833e-05
ichthyosis congenita, harlequin fetus type [NCBI] 3.0113e-05
weaver syndrome [NCBI] 2.80431e-05
APL [NCBI] 2.80431e-05
MKKS [NCBI] 2.41533e-05
EKV [NCBI] 2.36785e-05
thrombocytopenic purpura, autoimmune [NCBI] 2.18499e-05
AIRE [NCBI] 2.11737e-05
RTS [NCBI] 1.56528e-05
GJB2 [NCBI] 1.5095e-05
TNF [NCBI] 1.91005e-06
G6PD [NCBI] 1.47326e-06
EGF [NCBI] 2.88437e-07



Database Center for Life Science