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01 Ichthyosis [NCBI]

Gene


 Gene Link Information
Gain		 01
IPS [NCBI] 0.00112253
AREI [NCBI] 0.000367544
LI5 [NCBI] 0.000367544
INLNE [NCBI] 0.000367544
ARSC2 [NCBI] 0.000306807
MRX49 [NCBI] 0.000306807
GJB2 [NCBI] 0.000185213
KRT2 [NCBI] 0.000180408
TGM1 [NCBI] 0.000174732
ABHD5 [NCBI] 8.16672e-05
SPINK5 [NCBI] 7.96683e-05
STS [NCBI] 5.17792e-05
ST14 [NCBI] 4.77203e-05
LBR [NCBI] 3.79527e-05
XG [NCBI] 3.65543e-05
ERCC2 [NCBI] 3.64568e-05
LOR [NCBI] 3.27056e-05
NSDHL [NCBI] 3.22741e-05
CLDN1 [NCBI] 2.82067e-05
ERCC3 [NCBI] 2.73469e-05
CYP4F22 [NCBI] 2.65503e-05
VPS33B [NCBI] 2.05477e-05
PNPLA2 [NCBI] 1.84938e-05
KLK7 [NCBI] 1.63849e-05
GPR143 [NCBI] 1.60334e-05
KRT1 [NCBI] 1.5566e-05
FLG [NCBI] 1.48469e-05
ICHTHYIN [NCBI] 1.25283e-05
SNAP29 [NCBI] 1.25283e-05
GBA [NCBI] 1.23395e-05
ALOXE3 [NCBI] 1.16301e-05
C7orf11 [NCBI] 1.10469e-05
ALOX12B [NCBI] 1.02678e-05
NLGN4X [NCBI] 9.32887e-06
VCX [NCBI] 9.32887e-06
PRSS8 [NCBI] 9.15715e-06
CYP4F2 [NCBI] 9.15715e-06
IFI44 [NCBI] 8.72622e-06
ABCA2 [NCBI] 8.60375e-06
PRKCH [NCBI] 8.60375e-06
ARSE [NCBI] 8.48948e-06
NIPA1 [NCBI] 8.38237e-06
ALOX15B [NCBI] 8.18644e-06
ABCA12 [NCBI] 7.77701e-06
KLK5 [NCBI] 7.70573e-06
BGN [NCBI] 7.44717e-06
ABCA3 [NCBI] 6.57546e-06
CCRK [NCBI] 6.43778e-06
CDK7 [NCBI] 6.34142e-06
ALDH3A2 [NCBI] 6.19214e-06
GJB3 [NCBI] 6.08158e-06
KRT10 [NCBI] 5.88014e-06
PPOX [NCBI] 5.55746e-06
GJB6 [NCBI] 5.53801e-06
VKORC1 [NCBI] 5.42586e-06
GJA1 [NCBI] 5.33786e-06
KAL1 [NCBI] 5.30392e-06
MGP [NCBI] 4.49678e-06
BPI [NCBI] 3.98202e-06
HSPB1 [NCBI] 3.51407e-06
DHFR [NCBI] 2.64761e-06
NOD2 [NCBI] 2.15924e-06
ADA [NCBI] 1.90198e-06
CD68 [NCBI] 1.15222e-06
IL1RN [NCBI] 1.01535e-06
AFP [NCBI] 5.28551e-07
PTH [NCBI] 1.15782e-07
EGFR [NCBI] 1.09452e-07



OMIM


 OMIM Link Information
gain		 01
ichthyosis, x-linked [NCBI] 0.00351178
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.00328602
ichthyosis prematurity syndrome [NCBI] 0.0030116
SLS [NCBI] 0.00177644
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 0.00123763
exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like [NCBI] 0.000993831
LI1 [NCBI] 0.000992506
NLS [NCBI] 0.000895081
ichthyosis congenita, harlequin fetus type [NCBI] 0.000857135
NCIE1 [NCBI] 0.00082126
ichthyosis, bullous type [NCBI] 0.000793446
NETH [NCBI] 0.00079247
NNCI [NCBI] 0.000776146
ichthyosis vulgaris [NCBI] 0.000729562
NCR [NCBI] 0.000694153
LI5 [NCBI] 0.000694153
sabinas brittle hair syndrome [NCBI] 0.000694153
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 0.000693975
woolly hair, autosomal dominant [NCBI] 0.000641003
CDS [NCBI] 0.000625687
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000618151
IHCM [NCBI] 0.000616764
zunich neuroectodermal syndrome [NCBI] 0.000594588
trichorrhexis nodosa syndrome [NCBI] 0.000570168
peeling skin syndrome [NCBI] 0.000521852
TTDP [NCBI] 0.000484523
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 0.000449387
KRT2A [NCBI] 0.000437089
ichthyosis, lamellar, autosomal dominant [NCBI] 0.00035554
EKV [NCBI] 0.000345176
vohwinkel syndrome, variant form [NCBI] 0.000334225
TGM1 [NCBI] 0.000301636
SLE [NCBI] 0.000298752
ichthyosis--cheek--eyebrow syndrome [NCBI] 0.000296925
ichthyosis hystrix gravior [NCBI] 0.000296925
ichthyosis and male hypogonadism [NCBI] 0.000296925
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis [NCBI] 0.000296925
gaucher disease, perinatal lethal [NCBI] 0.00027943
alport syndrome, autosomal dominant [NCBI] 0.000255266
keratosis linearis with ichthyosis congenita and sclerosing keratoderma [NCBI] 0.000197868
ichthyosis, hystrix-like, with deafness [NCBI] 0.000197868
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis [NCBI] 0.000197868
congenital hemidysplasia with ichthyosiform erythroderma and limb defects [NCBI] 0.000179402
CDPX1 [NCBI] 0.000163161
CLDN1 [NCBI] 0.000160242
FLG [NCBI] 0.000148805
SPINK5 [NCBI] 0.000145805
GJB2 [NCBI] 0.000134831
MSD [NCBI] 0.000133552
LBR [NCBI] 0.00013056
TTDN1 [NCBI] 0.00013016
CDPX2 [NCBI] 0.000129363
TTDN1 [NCBI] 0.000103857
XPD [NCBI] 0.000100651
ST14 [NCBI] 0.000100199
ichthyosis, hepatosplenomegaly, and cerebellar degeneration [NCBI] 9.88934e-05
camptodactyly-ichthyosis syndrome [NCBI] 9.88934e-05
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [NCBI] 9.88934e-05
oral and digital anomalies with ichthyosis [NCBI] 9.88934e-05
trichodysplasia-xeroderma [NCBI] 9.88934e-05
ichthyosis with alopecia, eclabion, ectropion, and mental retardation [NCBI] 9.88934e-05
osteosclerosis with ichthyosis and fractures [NCBI] 9.88934e-05
ichthyosis, split hairs, and amino aciduria [NCBI] 9.88934e-05
ichthyosis with hypotrichosis, autosomal recessive [NCBI] 9.88934e-05
ichthyosis, mental retardation, dwarfism, and renal impairment [NCBI] 9.88934e-05
stormorken syndrome [NCBI] 9.88934e-05
ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin [NCBI] 9.88934e-05
PHA [NCBI] 8.44351e-05
GBA [NCBI] 8.40922e-05
KRT1 [NCBI] 8.06978e-05
sjogren-larsson-like ichthyosis without cns or eye involvement [NCBI] 7.6457e-05
GJB3 [NCBI] 7.35312e-05
ERCC2 [NCBI] 7.1116e-05
ARSC2 [NCBI] 7.08523e-05
RPL12 [NCBI] 7.08523e-05
SNAP29 [NCBI] 7.08523e-05
ZNF79 [NCBI] 7.08523e-05
arthrogryposis and ectodermal dysplasia [NCBI] 6.80112e-05
ALDH3A2 [NCBI] 6.52749e-05
OA1 [NCBI] 6.36632e-05
LI3 [NCBI] 6.25391e-05
keratitis, hereditary [NCBI] 5.84794e-05
KAL1 [NCBI] 5.83006e-05
ichthyin [NCBI] 5.70795e-05
SLC2A8 [NCBI] 5.70795e-05
ANGPTL2 [NCBI] 5.70795e-05
keratosis palmoplantaris striata i [NCBI] 5.52517e-05
GTF2H1 [NCBI] 5.1886e-05
keratoderma, palmoplantar, with deafness [NCBI] 5.02861e-05
STXBP1 [NCBI] 4.85161e-05
CD99 [NCBI] 4.85161e-05
epidermolysis bullosa dystrophica, pasini type [NCBI] 4.49346e-05
hyperprolinemia, type i [NCBI] 4.2179e-05
gaucher disease, type ii [NCBI] 3.98445e-05
XG [NCBI] 3.97072e-05
LOR [NCBI] 3.97072e-05
KEAP1 [NCBI] 3.97072e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 3.87993e-05
muckle-wells syndrome [NCBI] 3.87993e-05
EPPK [NCBI] 3.78218e-05
ED2 [NCBI] 3.6904e-05
LMX1B [NCBI] 3.59021e-05
KLK7 [NCBI] 3.59021e-05
ERCC3 [NCBI] 3.4442e-05
BGN [NCBI] 3.37867e-05
histidinemia [NCBI] 3.05029e-05
epidermolysis bullosa letalis [NCBI] 2.93959e-05
EBR1 [NCBI] 2.88731e-05
DAZ [NCBI] 2.65604e-05
RCDP1 [NCBI] 2.56754e-05
mannosidosis, alpha b, lysosomal [NCBI] 2.56754e-05
FDH [NCBI] 2.27531e-05
HEMB [NCBI] 1.0885e-05
PTH [NCBI] 9.86853e-06
EGFR [NCBI] 7.23185e-06
EV [NCBI] 6.64043e-06
DMD [NCBI] 4.73431e-06
DHFR [NCBI] 3.12914e-06
AFP [NCBI] 2.51137e-06
ADA [NCBI] 7.84432e-07



Database Center for Life Science