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MeSH keywords -> Related genes, diseases (OMIM)


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01 [NCBI]

Gene


 Gene Link Information
Gain		 01
TDD [NCBI] 0.000499621
SRD5A2 [NCBI] 0.000196425
AMH [NCBI] 0.000162884
AR [NCBI] 0.000131574
HSD17B3 [NCBI] 0.000120296
LHCGR [NCBI] 7.62446e-05
WT1 [NCBI] 6.81534e-05
HSD3B2 [NCBI] 5.2751e-05
AMHR2 [NCBI] 4.72863e-05
CYP17A1 [NCBI] 2.77022e-05
SRD5A1 [NCBI] 1.88386e-05
NR5A1 [NCBI] 1.81895e-05
STAR [NCBI] 1.43894e-05
SRY [NCBI] 1.16799e-05
SF1 [NCBI] 9.34128e-06
WTAP [NCBI] 8.66914e-06
SHBG [NCBI] 7.76243e-06
CYP11B1 [NCBI] 7.70449e-06
RBMY1A1 [NCBI] 7.32833e-06
WNT4 [NCBI] 7.02053e-06
NR0B1 [NCBI] 6.82155e-06
ATRX [NCBI] 6.5881e-06
PAX2 [NCBI] 5.4595e-06
NR3C1 [NCBI] 5.03247e-06
CYP19A1 [NCBI] 4.44268e-06
NPHS1 [NCBI] 4.14245e-06
EGR1 [NCBI] 3.63065e-06
CAT [NCBI] 1.75993e-06



OMIM


 OMIM Link Information
gain		 01
PPSH [NCBI] 0.00255436
TDD [NCBI] 0.00123814
AIS [NCBI] 0.00115914
HHG [NCBI] 0.00102023
LHCGR [NCBI] 0.000971131
megalencephaly [NCBI] 0.000938013
AMH [NCBI] 0.000823627
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 0.00072367
SRD5A2 [NCBI] 0.00063849
diaphragmatic hernia, congenital [NCBI] 0.00058575
reifenstein syndrome [NCBI] 0.000574792
PMDS [NCBI] 0.000544828
denys-drash syndrome [NCBI] 0.000496182
HSD17B3 [NCBI] 0.000404518
WT1 [NCBI] 0.000353319
AR [NCBI] 0.000347639
SLOS [NCBI] 0.000224435
AMHR2 [NCBI] 0.000193733
gynecomastia, familial [NCBI] 0.000190904
infertile male syndrome [NCBI] 0.000190904
genitopalatocardiac syndrome [NCBI] 0.000190904
CYP17A1 [NCBI] 0.000164877
frasier syndrome [NCBI] 0.000160001
WT1 [NCBI] 0.000117204
chondrodysplasia-pseudohermaphroditism syndrome [NCBI] 0.000110836
meacham syndrome [NCBI] 8.83803e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 8.69702e-05
macrocephaly [NCBI] 7.99154e-05
DSS [NCBI] 7.44244e-05
nephrotic syndrome, early-onset, with diffuse mesangial sclerosis [NCBI] 7.44244e-05
NR5A1 [NCBI] 7.40396e-05
cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome [NCBI] 7.03458e-05
pseudohermaphroditism, incomplete male, type i [NCBI] 6.7099e-05
CYP19A1 [NCBI] 6.63271e-05
por deficiency [NCBI] 5.82936e-05
sc phocomelia syndrome [NCBI] 5.66871e-05
wagr syndrome [NCBI] 5.52287e-05
SRY [NCBI] 5.50241e-05
hand-foot-uterus syndrome [NCBI] 5.26627e-05
STAR [NCBI] 5.10581e-05
marshall syndrome [NCBI] 5.04569e-05
methemoglobinemia due to deficiency of cytochrome b5 [NCBI] 4.95943e-05
HSD17B1 [NCBI] 4.95943e-05
SRD5A1 [NCBI] 4.70897e-05
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [NCBI] 4.68036e-05
ATRX [NCBI] 4.08067e-05
POR [NCBI] 3.96815e-05
SGBS1 [NCBI] 3.82728e-05
LHB [NCBI] 3.69729e-05
vitamin d-dependent rickets, type ii [NCBI] 3.69343e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 3.39282e-05
CYP11B1 [NCBI] 3.26007e-05
HAE [NCBI] 2.94109e-05
GPC3 [NCBI] 2.82319e-05
GCCR [NCBI] 2.73205e-05
coproporphyria [NCBI] 2.59732e-05
ATRX [NCBI] 2.57254e-05
SMAX1 [NCBI] 1.64059e-05
SHBG [NCBI] 1.43819e-05
DMD [NCBI] 1.31625e-05
CYP1A1 [NCBI] 1.07672e-05
VDR [NCBI] 1.32798e-06
CAT [NCBI] 1.61198e-07



Database Center for Life Science