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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypobetalipoproteinemias [NCBI]


Gene


Gene Link Information
Gain
01
FHBL2 [NCBI] 0.000499621
APOB [NCBI] 0.00036981
PCSK9 [NCBI] 1.80795e-05
MTTP [NCBI] 8.83348e-06
PANK2 [NCBI] 7.83861e-06
APOA1 [NCBI] 6.46819e-06
SERPINA1 [NCBI] 6.38411e-06
LDLR [NCBI] 5.41897e-06
CETP [NCBI] 4.07457e-06
HFE [NCBI] 3.35594e-06
LPL [NCBI] 3.31545e-06
APOE [NCBI] 2.09837e-06




OMIM


OMIM Link Information
gain
01
hypobetalipoproteinemia, familial, 2 [NCBI] 0.00390348
APOB [NCBI] 0.00266592
ABL [NCBI] 0.000461875
hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration [NCBI] 0.000108698
SLOS [NCBI] 0.000107369
anderson disease [NCBI] 0.000101342
CMRD [NCBI] 9.63076e-05
legg-calve-perthes disease [NCBI] 9.24751e-05
PCSK9 [NCBI] 4.8838e-05
SMAX1 [NCBI] 4.85035e-05
PANK2 [NCBI] 3.79639e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 2.76438e-05
RP [NCBI] 2.45732e-05
LPL [NCBI] 2.66222e-06
APOE [NCBI] 5.18362e-07




Database Center for Life Science