Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Disorders of Sex Development	[NCBI]

Gene	Link	Information Gain
AR	[NCBI]	0.000276867
VUR	[NCBI]	0.000189637
ZFY	[NCBI]	0.000166937
SRY	[NCBI]	0.000159656
SOX9	[NCBI]	9.62439e-05
AMH	[NCBI]	8.52909e-05
DMRT2	[NCBI]	2.43609e-05
DMRT1	[NCBI]	1.9059e-05
WNT4	[NCBI]	1.72109e-05
DMRT3	[NCBI]	1.33854e-05
DOCK8	[NCBI]	1.19037e-05
HSD17B3	[NCBI]	9.34497e-06
TBX3	[NCBI]	8.49167e-06
EFNB1	[NCBI]	8.30118e-06
AKR1C3	[NCBI]	8.12983e-06
LHCGR	[NCBI]	7.74259e-06
TSPY1	[NCBI]	7.46365e-06
FOXL2	[NCBI]	7.22408e-06
SRD5A2	[NCBI]	6.05117e-06
SHOX	[NCBI]	5.78618e-06
CYP17A1	[NCBI]	4.90747e-06

OMIM	Link	Information gain
AIS	[NCBI]	0.00167654
GBY	[NCBI]	0.000948879
gonadal dysgenesis, xy type	[NCBI]	0.000847142
AR	[NCBI]	0.000768813
AMH	[NCBI]	0.000473233
SRY	[NCBI]	0.000439943
GDXY	[NCBI]	0.000309343
campomelic dysplasia	[NCBI]	0.00028598
SOX9	[NCBI]	0.000196411
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	[NCBI]	0.000144621
SRA2	[NCBI]	0.000103088
h-y antigen receptor	[NCBI]	0.000102276
DSS	[NCBI]	8.83005e-05
acrogeria, gottron type	[NCBI]	8.83005e-05
camptomelic syndrome, long-limb type	[NCBI]	8.42118e-05
NR0B1	[NCBI]	7.94139e-05
TRS	[NCBI]	7.39071e-05
xx male syndrome	[NCBI]	7.39071e-05
reifenstein syndrome	[NCBI]	7.39071e-05
lenz-majewski hyperostotic dwarfism	[NCBI]	7.21095e-05
PMDS	[NCBI]	7.0493e-05
SLOS	[NCBI]	6.66304e-05
UMS	[NCBI]	6.05193e-05
donohue syndrome	[NCBI]	5.55972e-05
POF1	[NCBI]	5.55972e-05
ABS	[NCBI]	5.38804e-05
neuroblastoma stage 4s gene	[NCBI]	5.25107e-05
TBX3	[NCBI]	4.61902e-05
NR5A1	[NCBI]	3.5334e-05
CYP17A1	[NCBI]	3.23658e-05