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MeSH keywords -> Related genes, diseases (OMIM)


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01 Skin Diseases, Genetic [NCBI]

Gene


 Gene Link Information
Gain		 01
DUH [NCBI] 0.000623709
CDAGS [NCBI] 0.000381162
C8orf8 [NCBI] 0.000381162
SPG23 [NCBI] 0.000381162
EKV3 [NCBI] 0.000381162
TDH [NCBI] 0.000381162
C8orf12 [NCBI] 0.000381162
KWE [NCBI] 0.000320423
FERMT1 [NCBI] 0.000136255
GJB3 [NCBI] 9.0466e-05
HR [NCBI] 6.83782e-05
SPINK5 [NCBI] 2.89578e-05
ADAR [NCBI] 2.77464e-05
DSP [NCBI] 2.59958e-05
KRT6A [NCBI] 2.18113e-05
PKP1 [NCBI] 2.08232e-05
ECM1 [NCBI] 1.87433e-05
FLCN [NCBI] 1.8041e-05
KRT10 [NCBI] 1.7103e-05
GJB2 [NCBI] 1.64713e-05
XKR6 [NCBI] 1.63796e-05
AMAC1L2 [NCBI] 1.63796e-05
FAM167A [NCBI] 1.39992e-05
SLC29A3 [NCBI] 1.39992e-05
SCYL1BP1 [NCBI] 1.39992e-05
BLK [NCBI] 1.31008e-05
MTMR9 [NCBI] 1.25175e-05
KRT4 [NCBI] 1.20837e-05
EVPL [NCBI] 1.20837e-05
FERMT2 [NCBI] 1.20837e-05
FBLIM1 [NCBI] 1.17381e-05
GJB4 [NCBI] 1.14507e-05
KRT6C [NCBI] 1.06266e-05
LOR [NCBI] 1.03273e-05
KRT6B [NCBI] 1.01952e-05
NSDHL [NCBI] 1.01952e-05
PPL [NCBI] 9.74986e-06
ANTXR2 [NCBI] 9.65454e-06
RAB6A [NCBI] 9.47847e-06
ZMPSTE24 [NCBI] 9.10424e-06
CDSN [NCBI] 8.53728e-06
ATP2A2 [NCBI] 6.88139e-06
AIRE [NCBI] 6.80994e-06
TGM1 [NCBI] 6.65943e-06
SFN [NCBI] 6.47757e-06
KRT5 [NCBI] 6.39348e-06
DSG1 [NCBI] 6.33967e-06
ARNT [NCBI] 6.21221e-06
LAMB3 [NCBI] 4.44194e-06
MYC [NCBI] 4.0439e-06
ACE [NCBI] 2.82238e-06



OMIM


 OMIM Link Information
gain		 01
hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome [NCBI] 0.00114043
cdags syndrome [NCBI] 0.00092257
erythrokeratodermia variabilis 3 [NCBI] 0.000840405
keratolytic winter erythema [NCBI] 0.000787083
ATOD6 [NCBI] 0.000715905
SPG23 [NCBI] 0.000689681
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.000575369
EKV [NCBI] 0.000537865
APL [NCBI] 0.000456186
DDD [NCBI] 0.000249379
ectodermal dysplasia/skin fragility syndrome [NCBI] 0.000198429
GJB3 [NCBI] 0.000122134
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000116362
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis [NCBI] 0.000107412
keloids [NCBI] 9.89352e-05
BLK [NCBI] 9.47785e-05
PPL [NCBI] 9.47785e-05
PEPB [NCBI] 9.47785e-05
hyalinosis, infantile systemic [NCBI] 8.60827e-05
naegeli syndrome [NCBI] 8.33736e-05
MTMR9 [NCBI] 8.09985e-05
IHCM [NCBI] 7.90288e-05
PKP1 [NCBI] 7.24206e-05
ALUNC [NCBI] 7.15501e-05
EVPL [NCBI] 6.99095e-05
GJB4 [NCBI] 6.99095e-05
leiomyoma, hereditary multiple, of skin [NCBI] 6.93203e-05
GVM [NCBI] 6.93203e-05
NETH [NCBI] 6.73629e-05
KFSD [NCBI] 6.64672e-05
BHD [NCBI] 6.33145e-05
HNA [NCBI] 6.26148e-05
SPINK5 [NCBI] 6.05698e-05
KLK7 [NCBI] 5.97412e-05
HR [NCBI] 5.76039e-05
DSP [NCBI] 5.69829e-05
DAR [NCBI] 5.69196e-05
ECM1 [NCBI] 5.58467e-05
CDPX2 [NCBI] 5.5545e-05
DST [NCBI] 5.53239e-05
FDH [NCBI] 5.23746e-05
ARNT [NCBI] 5.22791e-05
aspartylglucosaminuria [NCBI] 5.08842e-05
RTS [NCBI] 4.88518e-05
APS1 [NCBI] 3.90032e-05
IP [NCBI] 3.46914e-05
PXE [NCBI] 2.67611e-05



Database Center for Life Science