Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Skin Diseases, Infectious [NCBI]

Gene


 Gene Link Information
Gain		 01
CXCL14 [NCBI] 1.33275e-05
DCD [NCBI] 1.29333e-05
MPO [NCBI] 1.20514e-05
PF4 [NCBI] 7.89663e-06
TPO [NCBI] 7.74524e-06
NOS2 [NCBI] 5.40192e-06
HGF [NCBI] 5.33621e-06
CDKN1A [NCBI] 4.0957e-06



OMIM


 OMIM Link Information
gain		 01
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum [NCBI] 0.000991404
NCR [NCBI] 0.000991404
hyperimmunoglobulin e-recurrent infection syndrome, autosomal recessive [NCBI] 0.000991404
EV [NCBI] 0.000267683
lymphoblastic transformation, intrinsic defect in [NCBI] 0.000140314
granulomatous disease with defect in neutrophil chemotaxis [NCBI] 0.000117844
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist [NCBI] 0.000103859
tuftsin deficiency [NCBI] 9.97657e-05
ichthyosis vulgaris [NCBI] 8.07952e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 7.77539e-05
SCN1 [NCBI] 7.60048e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 7.10508e-05
DCD [NCBI] 7.10164e-05
LAD [NCBI] 6.82623e-05
CHH [NCBI] 5.50831e-05
ITGB2 [NCBI] 5.35982e-05
MPO [NCBI] 4.19008e-05
MBL2 [NCBI] 3.52488e-05
PF4 [NCBI] 3.14811e-05
HGF [NCBI] 1.7369e-05
RA [NCBI] 1.1009e-05
SLE [NCBI] 4.85239e-06



Database Center for Life Science