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01 Alopecia [NCBI]

Gene


 Gene Link Information
Gain		 01
HR [NCBI] 0.000567933
HMU [NCBI] 0.000340315
TERC [NCBI] 0.000193108
VDR [NCBI] 0.000111086
AR [NCBI] 0.000100257
FOXN1 [NCBI] 7.91568e-05
SRD5A1 [NCBI] 2.82414e-05
KRT86 [NCBI] 2.27568e-05
GJB6 [NCBI] 2.1546e-05
SRD5A2 [NCBI] 2.05293e-05
CDSN [NCBI] 1.60612e-05
MS [NCBI] 1.53694e-05
KRT83 [NCBI] 1.46515e-05
FPR2 [NCBI] 1.44538e-05
CTSL1 [NCBI] 1.26107e-05
KRT5 [NCBI] 1.17464e-05
RBM28 [NCBI] 1.13732e-05
KRT14 [NCBI] 1.11014e-05
EDA2R [NCBI] 1.03565e-05
STX2 [NCBI] 1.00111e-05
CTF1 [NCBI] 1.00111e-05
LIPH [NCBI] 1.00111e-05
KRT81 [NCBI] 1.00111e-05
SVIL [NCBI] 1.00111e-05
DSG3 [NCBI] 9.68955e-06
TRH [NCBI] 9.12959e-06
SOX1 [NCBI] 8.90069e-06
SHH [NCBI] 8.43383e-06
SLC39A4 [NCBI] 8.02546e-06
LAMA5 [NCBI] 7.38155e-06
TRPS1 [NCBI] 7.25255e-06
LAMB1 [NCBI] 7.25255e-06
STS [NCBI] 7.19155e-06
EBP [NCBI] 7.02069e-06
TROVE2 [NCBI] 6.8572e-06
NR3C2 [NCBI] 6.76937e-06
BMP2 [NCBI] 6.72644e-06
LAMC1 [NCBI] 6.72329e-06
T [NCBI] 6.63474e-06
RECQL4 [NCBI] 6.63474e-06
COL17A1 [NCBI] 6.59214e-06
SHBG [NCBI] 6.34918e-06
CTNNB1 [NCBI] 6.22222e-06
CDK2 [NCBI] 6.11195e-06
CD34 [NCBI] 6.08702e-06
SMO [NCBI] 5.99602e-06
BAX [NCBI] 5.73911e-06
NCOA4 [NCBI] 5.46851e-06
AIRE [NCBI] 5.10271e-06
DKK1 [NCBI] 5.08553e-06
GHRH [NCBI] 5.05168e-06
EDA [NCBI] 5.03502e-06
POLG [NCBI] 4.98601e-06
BMI1 [NCBI] 4.83246e-06
PRL [NCBI] 4.78562e-06
SFN [NCBI] 4.77484e-06
RAG2 [NCBI] 4.47799e-06
NF1 [NCBI] 4.46624e-06
VCAN [NCBI] 4.35315e-06
CCR4 [NCBI] 4.03685e-06
SAT2 [NCBI] 4.0279e-06
TGFB2 [NCBI] 3.91598e-06
HDAC1 [NCBI] 3.85883e-06
IL6ST [NCBI] 3.55366e-06
CKAP4 [NCBI] 3.34409e-06
HSPB1 [NCBI] 3.27096e-06
OSM [NCBI] 3.24914e-06
ATR [NCBI] 2.97279e-06
XIAP [NCBI] 2.93277e-06
HLA-DQA1 [NCBI] 2.92839e-06
CFLAR [NCBI] 2.91967e-06
RAG1 [NCBI] 2.81885e-06
GJB1 [NCBI] 2.78276e-06
TGFB1 [NCBI] 2.74114e-06
TP63 [NCBI] 2.66124e-06
IGF1 [NCBI] 2.56954e-06
ATM [NCBI] 2.46425e-06
SMAD4 [NCBI] 2.42671e-06
CDKN2A [NCBI] 2.10856e-06
GJB2 [NCBI] 2.03722e-06
LIF [NCBI] 1.9895e-06
HLA-DQB1 [NCBI] 1.79723e-06
HLA-DRB1 [NCBI] 1.2806e-06
SOD1 [NCBI] 1.2576e-06
PTH [NCBI] 1.13089e-06
IL6 [NCBI] 1.06215e-06
IL1RN [NCBI] 8.32015e-07
AKT1 [NCBI] 7.44982e-07
FASLG [NCBI] 4.35761e-07
EPO [NCBI] 4.18339e-07
CASP3 [NCBI] 1.73544e-07
CDKN1A [NCBI] 1.09915e-07
PTGS2 [NCBI] 4.54435e-08
EGF [NCBI] 1.96835e-08



OMIM


 OMIM Link Information
gain		 01
alopecia, androgenetic [NCBI] 0.00908446
gapo syndrome [NCBI] 0.00636982
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.0043106
johnson neuroectodermal syndrome [NCBI] 0.00316334
hypotrichosis, marie unna type [NCBI] 0.00313163
alopecia-mental retardation syndrome 1 [NCBI] 0.00236858
mucoepithelial dysplasia, hereditary [NCBI] 0.00236858
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome [NCBI] 0.00236858
APL [NCBI] 0.00230654
CARASIL [NCBI] 0.00203669
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality [NCBI] 0.00157646
scholte syndrome [NCBI] 0.00157646
ALUNC [NCBI] 0.00118614
HR [NCBI] 0.000960531
alopecia-mental retardation syndrome 2 [NCBI] 0.000786952
BZX [NCBI] 0.000736714
PCOS1 [NCBI] 0.000719822
alopecia areata 1 [NCBI] 0.000643117
vitamin d-dependent rickets, type ii [NCBI] 0.000607478
VDR [NCBI] 0.000542277
vitamin d-dependent rickets, type ii, with normal vitamin d receptor [NCBI] 0.000488822
coffin-siris syndrome [NCBI] 0.000481372
onychotrichodysplasia and neutropenia [NCBI] 0.000436447
oculodentoosseous dysplasia, recessive [NCBI] 0.000436447
bullous dystrophy, hereditary macular type [NCBI] 0.000436447
alopecia-epilepsy-oligophrenia syndrome of moynahan [NCBI] 0.000381725
polyposis, skin pigmentation, alopecia, and fingernail changes [NCBI] 0.000381725
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina [NCBI] 0.000367161
anosmia, congenital [NCBI] 0.000367161
schopf-schulz-passarge syndrome [NCBI] 0.000320396
cerebellotrigeminal dermal dysplasia [NCBI] 0.000319904
KFSD [NCBI] 0.000300431
AR [NCBI] 0.000296684
APS2 [NCBI] 0.000257323
facial ectodermal dysplasia [NCBI] 0.0002342
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.0002342
loose anagen hair syndrome [NCBI] 0.000218912
ACC [NCBI] 0.000205789
t-cell immunodeficiency, congenital alopecia, and nail dystrophy [NCBI] 0.000190731
alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism [NCBI] 0.000159822
satoyoshi syndrome [NCBI] 0.000145876
MADA [NCBI] 0.000136496
AH [NCBI] 0.000136317
IP [NCBI] 0.000135314
BJS [NCBI] 0.000129002
FOXN1 [NCBI] 0.000125568
hypotrichosis simplex of scalp [NCBI] 0.000123068
SRD5A1 [NCBI] 0.000111113
monilethrix [NCBI] 0.000109974
SLE [NCBI] 0.000109429
KRTHB6 [NCBI] 0.000102947
SFN [NCBI] 9.72004e-05
OTD [NCBI] 9.53331e-05
alopecia congenita with keratosis palmoplantaris [NCBI] 9.53331e-05
hypogonadism, primary, and partial alopecia [NCBI] 9.53331e-05
alopecia, familial focal [NCBI] 9.53331e-05
CASS [NCBI] 9.53331e-05
alopecia universalis congenita, xy gonadal dysgenesis, and laryngomalacia [NCBI] 9.53331e-05
alopecia, congenital [NCBI] 9.53331e-05
ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [NCBI] 9.53331e-05
parc syndrome [NCBI] 9.53331e-05
ichthyosis with alopecia, eclabion, ectropion, and mental retardation [NCBI] 9.53331e-05
deafness-craniofacial syndrome [NCBI] 9.53331e-05
ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet [NCBI] 9.53331e-05
acrocephalopolysyndactyly type iii [NCBI] 9.53331e-05
woolly hair, hypotrichosis, everted lower lip, and outstanding ears [NCBI] 9.53331e-05
KRT17 [NCBI] 9.08651e-05
AOS [NCBI] 8.98387e-05
ED2 [NCBI] 8.96663e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 8.96663e-05
holocarboxylase synthetase deficiency [NCBI] 8.78562e-05
HGPS [NCBI] 8.46291e-05
CTSL [NCBI] 7.80578e-05
AEZ [NCBI] 7.75131e-05
TERC [NCBI] 7.71391e-05
spondyloepimetaphyseal dysplasia with hypotrichosis [NCBI] 7.29057e-05
BPH [NCBI] 7.29057e-05
ectodermal dysplasia, trichoodontoonychial type [NCBI] 7.29057e-05
aplasia cutis congenita, high myopia, and cone-rod dysfunction [NCBI] 7.29057e-05
noonan-like syndrome with loose anagen hair [NCBI] 7.29057e-05
KRTHB3 [NCBI] 7.22225e-05
COL17A1 [NCBI] 7.10245e-05
CYP17A1 [NCBI] 6.85626e-05
ODDD [NCBI] 6.70507e-05
CDPX2 [NCBI] 6.61822e-05
alopecia-contractures-dwarfism mental retardation syndrome [NCBI] 6.44687e-05
syringomas, multiple [NCBI] 6.44687e-05
multiple pterygium syndrome, aslan type [NCBI] 6.44687e-05
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 5.90056e-05
HJMD [NCBI] 5.90056e-05
eem syndrome [NCBI] 5.90056e-05
glomerulonephritis with sparse hair and telangiectases [NCBI] 5.90056e-05
PURE&apos [NCBI] 5.49549e-05
EPHB3 [NCBI] 5.32541e-05
chromosome 18p deletion syndrome [NCBI] 5.17361e-05
aplasia cutis congenita with epibulbar dermoids [NCBI] 5.17361e-05
DPR [NCBI] 5.17361e-05
CHRD [NCBI] 4.98832e-05
PTPN6 [NCBI] 4.98832e-05
SHH [NCBI] 4.94039e-05
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 4.90669e-05
CLCN2 [NCBI] 4.53837e-05
SLC39A4 [NCBI] 4.37261e-05
RXRA [NCBI] 4.37261e-05
sc phocomelia syndrome [NCBI] 4.14638e-05
FPRL1 [NCBI] 3.99692e-05
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 3.87261e-05
mast cell disease [NCBI] 3.75231e-05
XPD [NCBI] 3.53732e-05
GVM [NCBI] 3.53732e-05
GAD2 [NCBI] 3.39485e-05
IL1RN [NCBI] 3.39485e-05
CDSN [NCBI] 3.34029e-05
GJB6 [NCBI] 3.28864e-05
EDA [NCBI] 3.28864e-05
NOTCH1 [NCBI] 3.2396e-05
TTDP [NCBI] 3.18316e-05
CDKN1A [NCBI] 3.14843e-05
SRD5A2 [NCBI] 3.14843e-05
ERCC2 [NCBI] 2.98852e-05
GABEB [NCBI] 2.96472e-05
TRPS1 [NCBI] 2.96472e-05
SCD [NCBI] 2.91757e-05
HSS [NCBI] 2.89874e-05
VEGF [NCBI] 2.79074e-05
biotinidase deficiency [NCBI] 2.662e-05
POLG [NCBI] 2.6255e-05
HDAC1 [NCBI] 2.6007e-05
PPSH [NCBI] 2.45994e-05
CRC [NCBI] 2.38725e-05
RCDP1 [NCBI] 2.24372e-05
DKC [NCBI] 2.12925e-05
obesity [NCBI] 2.02415e-05
FDH [NCBI] 1.95866e-05
AIRE [NCBI] 1.88703e-05
PPARG [NCBI] 1.88703e-05
ED1 [NCBI] 1.70079e-05
CDK2 [NCBI] 1.67856e-05
ATM [NCBI] 1.64399e-05
prostate cancer [NCBI] 1.55564e-05
SHBG [NCBI] 1.4836e-05
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 1.46827e-05
hypertension, essential [NCBI] 1.44747e-05
CHH [NCBI] 1.31213e-05
FGF7 [NCBI] 1.00529e-05
EGF [NCBI] 9.18138e-06
APS1 [NCBI] 8.57434e-06
CEACAM5 [NCBI] 8.16757e-06
SMAX1 [NCBI] 4.95548e-06
AIS [NCBI] 3.18307e-06
PRL [NCBI] 2.73037e-06
EPO [NCBI] 1.26704e-06
PTH [NCBI] 1.03828e-06
ALD [NCBI] 2.6693e-07
AT [NCBI] 5.06221e-08
KLK3 [NCBI] 2.64027e-08



Database Center for Life Science