Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Disorders of Sex Development [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science