Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Scalp Dermatoses [NCBI]

Gene


 Gene Link Information
Gain		 01
DSG4 [NCBI] 1.40763e-05
HLA-C [NCBI] 9.46535e-06
BMP2 [NCBI] 7.92654e-06
GJB2 [NCBI] 7.67354e-06
PCNA [NCBI] 5.24357e-06
PTH [NCBI] 4.5905e-06



OMIM


 OMIM Link Information
gain		 01
ameloonychohypohidrotic syndrome [NCBI] 0.00129156
spiegler-brooke syndrome [NCBI] 0.00078076
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.000725612
alopecia, androgenetic [NCBI] 0.000306358
perifolliculitis capitis abscedens et suffodiens, familial [NCBI] 0.000141395
cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness [NCBI] 0.000141395
CVG/MR [NCBI] 0.000100846
ichthyosis, bullous type [NCBI] 9.25519e-05
complement component 5 deficiency [NCBI] 8.70992e-05
ichthyosis vulgaris [NCBI] 8.18742e-05
NETH [NCBI] 7.88324e-05
CYLD [NCBI] 7.88324e-05
KFSD [NCBI] 7.79339e-05
PDP [NCBI] 7.62745e-05
DSG4 [NCBI] 7.34161e-05
OFD1 [NCBI] 7.15296e-05
ichthyosis, x-linked [NCBI] 5.18201e-05
ALD [NCBI] 2.81442e-05
temporal arteritis [NCBI] 2.68225e-05
PCNA [NCBI] 1.80307e-05
PTH [NCBI] 1.45161e-05



Database Center for Life Science