Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperparathyroidism, Secondary	[NCBI]

Gene	Link	Information Gain
PTH	[NCBI]	0.00450778
VDR	[NCBI]	0.000198459
FGF23	[NCBI]	0.000102432
CASR	[NCBI]	5.18757e-05
ACP5	[NCBI]	2.21723e-05
MEN1	[NCBI]	1.17947e-05
TNFRSF11B	[NCBI]	1.12289e-05
EPO	[NCBI]	8.19276e-06
HNRNPD	[NCBI]	5.31732e-06
BMP7	[NCBI]	4.78438e-06
CYP27B1	[NCBI]	4.44527e-06
CHGA	[NCBI]	4.10681e-06
PTHLH	[NCBI]	3.95507e-06
CDKN1B	[NCBI]	3.7406e-06
CDKN2C	[NCBI]	3.39892e-06
CDC73	[NCBI]	3.33483e-06
FGF3	[NCBI]	2.56639e-06
PRKAR1A	[NCBI]	2.52953e-06
IGFBP1	[NCBI]	2.26513e-06
ITGB1	[NCBI]	2.1316e-06
CST3	[NCBI]	1.8132e-06
EGF	[NCBI]	1.69578e-06
ALB	[NCBI]	9.10431e-07
CYP3A4	[NCBI]	8.4039e-07
ENG	[NCBI]	7.529e-07
PTK2	[NCBI]	5.39522e-07
PCNA	[NCBI]	4.24086e-07
TNFRSF11A	[NCBI]	3.78429e-07
TNFSF11	[NCBI]	2.60286e-07
CETP	[NCBI]	2.03556e-07
BAX	[NCBI]	1.80057e-07
CDKN1A	[NCBI]	8.32502e-08
TRH	[NCBI]	7.18883e-08
ACE	[NCBI]	5.52031e-08
LPL	[NCBI]	3.75232e-09
EGFR	[NCBI]	3.08259e-09
CD68	[NCBI]	1.48301e-10
NOS3	[NCBI]	6.72206e-11

OMIM	Link	Information gain
PTH	[NCBI]	0.0171052
VDR	[NCBI]	0.000568719
vitamin d-dependent rickets, type ii	[NCBI]	0.000287819
EGF	[NCBI]	0.000131049
hyperparathyroidism, primary, caused by water clear cell hyperplasia	[NCBI]	0.000127588
CASR	[NCBI]	0.00012404
FGF23	[NCBI]	8.37112e-05
EGFR	[NCBI]	7.50273e-05
BGLAP	[NCBI]	7.23528e-05
hypophosphatemic rickets, x-linked dominant	[NCBI]	7.03443e-05
MEN2A	[NCBI]	6.1305e-05
GAS	[NCBI]	4.43636e-05
AVP	[NCBI]	3.94869e-05
polycystic kidneys	[NCBI]	3.79657e-05
PCNA	[NCBI]	3.66342e-05
CD	[NCBI]	2.93071e-05
IL6ST	[NCBI]	2.67912e-05
LPL	[NCBI]	2.1519e-05
TNFRSF11B	[NCBI]	1.05444e-05
LIPC	[NCBI]	7.66019e-06
PTK2	[NCBI]	2.2256e-06
MEN1	[NCBI]	2.20188e-06
EPO	[NCBI]	2.13267e-06
ALB	[NCBI]	8.35476e-07
ACP5	[NCBI]	6.98276e-07
SLE	[NCBI]	5.89232e-08
ABCC1	[NCBI]	1.87422e-08
PTHLH	[NCBI]	1.01688e-09