Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Protein Deficiency [NCBI]


Gene


Gene Link Information
Gain
01
PSAP [NCBI] 5.15562e-05
ACHE [NCBI] 1.6386e-05
EPO [NCBI] 1.34364e-05
TTR [NCBI] 1.2498e-05
CHAT [NCBI] 1.18719e-05
SLC5A3 [NCBI] 1.0094e-05
CAT [NCBI] 9.72054e-06
PC [NCBI] 8.92106e-06
HAPLN1 [NCBI] 8.714e-06
WFDC5 [NCBI] 8.58009e-06
TTPA [NCBI] 8.03365e-06
SERPING1 [NCBI] 7.77392e-06
IGFBP3 [NCBI] 6.17117e-06
PON1 [NCBI] 5.17566e-06
F2 [NCBI] 5.05952e-06
F5 [NCBI] 4.70618e-06
CETP [NCBI] 4.31922e-06
ADA [NCBI] 4.30704e-06
TRH [NCBI] 3.94477e-06
LPL [NCBI] 3.55517e-06
MBP [NCBI] 3.2012e-06
TGFB1 [NCBI] 2.80836e-06
CDKN1A [NCBI] 2.00851e-06
TNF [NCBI] 8.12137e-07




OMIM


OMIM Link Information
gain
01
tay-sachs disease, ab variant [NCBI] 0.000107666
enterokinase deficiency [NCBI] 0.000105561
metachromatic leukodystrophy due to saposin b deficiency [NCBI] 9.7782e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 8.13856e-05
TGD [NCBI] 7.85232e-05
HAE [NCBI] 6.97197e-05
ABL [NCBI] 6.94508e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 6.67567e-05
TSD [NCBI] 5.08561e-05
ACHE [NCBI] 4.73701e-05
CD47 [NCBI] 4.49227e-05
TBG [NCBI] 4.44511e-05
PROS1 [NCBI] 4.06731e-05
TTR [NCBI] 3.85198e-05
CHAT [NCBI] 3.6939e-05
PC [NCBI] 3.56351e-05
GPT [NCBI] 3.54495e-05
EPO [NCBI] 3.23181e-05
PON1 [NCBI] 2.91757e-05
CAT [NCBI] 2.60026e-05
SPINK1 [NCBI] 2.50387e-05
AVP [NCBI] 1.87644e-05
LPL [NCBI] 6.76066e-06
CRH [NCBI] 5.3633e-06
MBP [NCBI] 4.7374e-06
CF [NCBI] 2.32532e-06
VEGF [NCBI] 1.10356e-06
TNF [NCBI] 5.63063e-07




Database Center for Life Science