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01 Hypotrichosis [NCBI]

Gene


 Gene Link Information
Gain		 01
HMU [NCBI] 0.000817003
HTS [NCBI] 0.000401057
RMRP [NCBI] 0.000250275
DSG4 [NCBI] 0.000187731
LIPH [NCBI] 6.05522e-05
LPAR4 [NCBI] 5.89016e-05
CDH3 [NCBI] 5.85741e-05
ST14 [NCBI] 5.70274e-05
P2RY5 [NCBI] 4.31372e-05
HR [NCBI] 3.13561e-05
EDA [NCBI] 2.70469e-05
CDSN [NCBI] 2.02231e-05
EPB49 [NCBI] 1.24282e-05
SOX18 [NCBI] 1.11429e-05
PRSS8 [NCBI] 1.0971e-05
CDH4 [NCBI] 1.0195e-05
EDAR [NCBI] 9.51688e-06
PKP1 [NCBI] 9.51688e-06
PKP2 [NCBI] 9.3188e-06
TRPS1 [NCBI] 9.3188e-06
CLDN1 [NCBI] 9.25756e-06
PCDH15 [NCBI] 9.25756e-06
CDH23 [NCBI] 8.98047e-06
TGIF1 [NCBI] 8.83348e-06
DSP [NCBI] 7.08372e-06
DSG1 [NCBI] 6.68139e-06
TGFB2 [NCBI] 5.94167e-06
PCNA [NCBI] 5.56241e-06
IFNGR1 [NCBI] 4.22234e-06



OMIM


 OMIM Link Information
gain		 01
hypotrichosis, marie unna type [NCBI] 0.0064253
BZX [NCBI] 0.00360182
schopf-schulz-passarge syndrome [NCBI] 0.00207247
hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome [NCBI] 0.000959695
hypotrichosis simplex [NCBI] 0.000959695
LAH3 [NCBI] 0.000959695
hypotrichosis simplex of scalp [NCBI] 0.000721967
onychotrichodysplasia and neutropenia [NCBI] 0.000607072
DSG4 [NCBI] 0.000567624
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.000510391
HJMD [NCBI] 0.000510346
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000367231
LAH [NCBI] 0.00034558
AH [NCBI] 0.000327499
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis [NCBI] 0.000254219
uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly [NCBI] 0.000254219
CDH3 [NCBI] 0.000224554
arthrogryposis and ectodermal dysplasia [NCBI] 0.00022327
CDSN [NCBI] 0.000183533
LIPH [NCBI] 0.000176747
OTD [NCBI] 0.000126878
ichthyosis with hypotrichosis, autosomal recessive [NCBI] 0.000126878
trichoodontoonychial dysplasia [NCBI] 0.000126878
hypotrichosis-lymphedema-telangiectasia syndrome [NCBI] 0.000126878
rombo syndrome [NCBI] 0.000104412
ectodermal dysplasia, trichoodontoonychial type [NCBI] 0.000104412
spondyloepimetaphyseal dysplasia with hypotrichosis [NCBI] 0.000104412
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis [NCBI] 9.59359e-05
eem syndrome [NCBI] 9.0434e-05
SENP2 [NCBI] 8.81249e-05
MAP3K13 [NCBI] 8.81249e-05
PURE&apos [NCBI] 8.63444e-05
TRPS3 [NCBI] 8.30867e-05
SOX18 [NCBI] 7.43456e-05
ALUNC [NCBI] 6.85628e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 6.438e-05
TRPS1 [NCBI] 6.03371e-05
ST14 [NCBI] 5.95952e-05
AEZ [NCBI] 5.83269e-05
CLDN1 [NCBI] 5.81716e-05
RMRP [NCBI] 5.58217e-05
FLT4 [NCBI] 5.23317e-05
PCNA [NCBI] 1.75011e-05



Database Center for Life Science