Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hoarseness [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000828242
ECM1 [NCBI] 4.26308e-05
ASAH1 [NCBI] 2.69048e-05
MS [NCBI] 2.06195e-05
CTNNBIP1 [NCBI] 1.35804e-05
CDH1 [NCBI] 8.01927e-06
BMP2 [NCBI] 7.64014e-06



OMIM


 OMIM Link Information
gain		 01
neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux [NCBI] 0.00107364
leri pleonosteosis [NCBI] 0.000938013
dubowitz syndrome [NCBI] 0.00063878
dwarfism with stiff joints and ocular abnormalities [NCBI] 0.000127588
subaortic stenosis--short stature syndrome [NCBI] 0.000127588
GEMSS [NCBI] 0.000119107
subglottic bar [NCBI] 0.000109506
growth-mental deficiency syndrome of myhre [NCBI] 9.73745e-05
PC1 [NCBI] 9.16802e-05
ECM1 [NCBI] 8.91456e-05
UMS [NCBI] 8.5726e-05
lipoid proteinosis of urbach and wiethe [NCBI] 8.20324e-05
SGBS1 [NCBI] 7.69732e-05
SLE [NCBI] 5.9309e-06
RA [NCBI] 1.2981e-06



Database Center for Life Science