Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Smith-Lemli-Opitz Syndrome	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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