Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Hirsutism [NCBI]


Gene


Gene Link Information
Gain
01
SHBG [NCBI] 0.000472263
PRL [NCBI] 7.10745e-05
CYP21A2 [NCBI] 4.10856e-05
HSD3B2 [NCBI] 2.95338e-05
AR [NCBI] 2.33866e-05
CAPN10 [NCBI] 1.52809e-05
KLK3 [NCBI] 1.41063e-05
NR3C1 [NCBI] 1.2915e-05
INSR [NCBI] 1.28716e-05
GIP [NCBI] 1.11157e-05
SORBS1 [NCBI] 1.07035e-05
FSHB [NCBI] 1.00516e-05
INS [NCBI] 9.94403e-06
HSD17B2 [NCBI] 8.65068e-06
SRD5A1 [NCBI] 8.42692e-06
IRS1 [NCBI] 8.38886e-06
CYP11A1 [NCBI] 7.60953e-06
AKR1C2 [NCBI] 7.09121e-06
STAR [NCBI] 6.23356e-06
SRD5A2 [NCBI] 5.91906e-06
CRH [NCBI] 5.2676e-06
ADRB3 [NCBI] 5.18351e-06
CP [NCBI] 4.5182e-06
ETV6 [NCBI] 4.2082e-06
PPARG [NCBI] 3.12524e-06
TNFSF11 [NCBI] 2.67398e-06
TNFRSF11B [NCBI] 2.63506e-06
TRH [NCBI] 2.20631e-06




OMIM


OMIM Link Information
gain
01
PCOS1 [NCBI] 0.00690869
SHBG [NCBI] 0.00199536
dyssegmental dysplasia, rolland-desbuquois type [NCBI] 0.00129172
cerebellar hypoplasia, mental retardation, and quadrupedal locomotion [NCBI] 0.000694153
hypertrichosis universalis [NCBI] 0.000570168
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.000442837
schinzel-giedion midface-retraction syndrome [NCBI] 0.000400267
coffin-siris syndrome [NCBI] 0.000328512
hirsutism--skeletal dysplasia--mental retardation syndrome [NCBI] 0.000274036
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 0.000178596
diabetes mellitus, insulin-resistant, with acanthosis nigricans [NCBI] 0.000178596
PRL [NCBI] 0.000169231
cyprus facial neuromusculoskeletal syndrome [NCBI] 0.000136591
hypersecretion of adrenal androgens, familial [NCBI] 0.000136591
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 0.000132213
alopecia, androgenetic [NCBI] 0.000118136
fibromatosis, gingival, with hypertrichosis and mental retardation [NCBI] 0.000114122
CDLS1 [NCBI] 0.000110348
CYP11A1 [NCBI] 0.000103546
barber-say syndrome [NCBI] 9.6046e-05
cortisone reductase deficiency [NCBI] 9.6046e-05
floating-harbor syndrome [NCBI] 8.39246e-05
INSR [NCBI] 8.28384e-05
FMD [NCBI] 7.40438e-05
CNC1 [NCBI] 6.09211e-05
AR [NCBI] 4.85609e-05
SRD5A1 [NCBI] 4.76758e-05
EIG [NCBI] 3.92096e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 3.6797e-05
KLK3 [NCBI] 3.33918e-05
SRD5A2 [NCBI] 3.1778e-05
NR5A1 [NCBI] 3.05538e-05
GIP [NCBI] 3.01413e-05
GCCR [NCBI] 2.78948e-05
GDXY [NCBI] 2.78948e-05
NR0B1 [NCBI] 2.78948e-05
GNRH1 [NCBI] 2.54622e-05
glycogen storage disease i [NCBI] 2.25207e-05
porphyria cutanea tarda [NCBI] 2.21999e-05
TNF [NCBI] 2.18282e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 2.10191e-05
STAR [NCBI] 1.9379e-05
SERPINA6 [NCBI] 1.72411e-05
CRH [NCBI] 1.33762e-05
CP [NCBI] 1.02676e-05
SLE [NCBI] 9.43832e-06




Database Center for Life Science