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01 Smith-Lemli-Opitz Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
DHCR7 [NCBI] 0.000722403
MID1 [NCBI] 0.000102969
SHH [NCBI] 7.27975e-05
MID2 [NCBI] 5.54782e-05
CYP27A1 [NCBI] 3.20387e-05
SC5DL [NCBI] 2.70391e-05
MID1IP1 [NCBI] 1.58891e-05
IGBP1 [NCBI] 1.15934e-05
GRM8 [NCBI] 1.12478e-05
NR1H3 [NCBI] 1.11606e-05
LBR [NCBI] 8.00071e-06
HTR1A [NCBI] 7.74034e-06
SMO [NCBI] 7.22371e-06
NTN1 [NCBI] 7.13686e-06
ATRX [NCBI] 7.08134e-06
SREBF2 [NCBI] 6.97547e-06
LYN [NCBI] 4.91206e-06
PAX6 [NCBI] 4.42937e-06
AFP [NCBI] 4.41886e-06
LDLR [NCBI] 4.09366e-06
APOE [NCBI] 3.92306e-06



OMIM


 OMIM Link Information
gain		 01
SLOS [NCBI] 0.0167514
DHCR7 [NCBI] 0.00179458
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.0013334
hypobetalipoproteinemia, familial, 2 [NCBI] 0.000938013
lathosterolosis [NCBI] 0.000270223
MID1 [NCBI] 0.000194577
SHH [NCBI] 0.000156687
hydrops-ectopic calcification-moth-eaten skeletal dysplasia [NCBI] 0.000123456
MVK [NCBI] 9.89055e-05
midline 2 [NCBI] 8.21209e-05
GRM8 [NCBI] 8.21209e-05
CDPX2 [NCBI] 7.92456e-05
SC5DL [NCBI] 6.83427e-05
desmosterolosis [NCBI] 5.84447e-05
congenital hemidysplasia with ichthyosiform erythroderma and limb defects [NCBI] 4.41076e-05
sitosterolemia [NCBI] 4.19267e-05
HIDS [NCBI] 3.54167e-05
PHA [NCBI] 3.41519e-05
PHS [NCBI] 2.60285e-05
ABL [NCBI] 2.11863e-05
SMS [NCBI] 1.35105e-05
APOE [NCBI] 1.26278e-05
AFP [NCBI] 1.0035e-05



Database Center for Life Science