Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Sheep Diseases	[NCBI]

Gene	Link	Information Gain
MEG3	[NCBI]	0.000330389
CTSL1	[NCBI]	3.7434e-05
PRL	[NCBI]	2.99906e-05
ACHE	[NCBI]	2.19625e-05
GDF9	[NCBI]	2.11424e-05
ALB	[NCBI]	1.24893e-05
TF	[NCBI]	1.23076e-05
MCEE	[NCBI]	1.20977e-05
HYAL2	[NCBI]	9.96529e-06
STOM	[NCBI]	9.75058e-06
BMP15	[NCBI]	9.6846e-06
UROD	[NCBI]	8.51273e-06
INSL3	[NCBI]	7.47111e-06
PLG	[NCBI]	6.56092e-06
MAP2	[NCBI]	6.40287e-06
PCNA	[NCBI]	6.13051e-06
SCGB1A1	[NCBI]	5.64222e-06
MATN1	[NCBI]	5.58912e-06
INS	[NCBI]	5.16134e-06
IL2	[NCBI]	5.04437e-06
FGFR3	[NCBI]	4.71906e-06
PTGS1	[NCBI]	3.99488e-06
CCK	[NCBI]	3.40706e-06
TLR4	[NCBI]	3.37722e-06
CAT	[NCBI]	3.23209e-06
AVP	[NCBI]	3.09224e-06
CD68	[NCBI]	2.98013e-06
TNF	[NCBI]	2.72361e-06

OMIM	Link	Information gain
LIP	[NCBI]	0.000830168
hyperbilirubinemia, conjugated, type iii	[NCBI]	0.000140314
thyroid hormonogenesis, genetic defect in, 5	[NCBI]	9.37927e-05
neuraminidase deficiency with beta-galactosidase deficiency	[NCBI]	8.47446e-05
PRL	[NCBI]	8.03003e-05
ehlers-danlos syndrome, type vii, autosomal recessive	[NCBI]	7.97164e-05
neural tube defects	[NCBI]	7.10508e-05
gm1-gangliosidosis, type i	[NCBI]	6.77584e-05
ACHE	[NCBI]	6.48777e-05
HYAL2	[NCBI]	5.75277e-05
MEG3	[NCBI]	5.2444e-05
BMP15	[NCBI]	5.2444e-05
IL5	[NCBI]	4.40399e-05
ALB	[NCBI]	4.21183e-05
TF	[NCBI]	4.19159e-05
GLB1	[NCBI]	3.76234e-05
CCL2	[NCBI]	3.28373e-05
BWS	[NCBI]	3.17359e-05
polycystic kidneys	[NCBI]	2.87097e-05
GAL	[NCBI]	2.57757e-05
PLG	[NCBI]	2.33663e-05
INS	[NCBI]	1.99248e-05
FGFR3	[NCBI]	1.90183e-05
IL2	[NCBI]	1.67218e-05
SHH	[NCBI]	1.56569e-05
TLR4	[NCBI]	1.49384e-05
CJD	[NCBI]	1.35487e-05
PCNA	[NCBI]	8.72422e-06
CCK	[NCBI]	5.63121e-06
CAT	[NCBI]	5.24694e-06
CRH	[NCBI]	3.69965e-06
AVP	[NCBI]	2.56346e-06
VEGF	[NCBI]	2.533e-06
TNF	[NCBI]	1.94188e-06