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01 Hypopituitarism [NCBI]

Gene


 Gene Link Information
Gain		 01
POU1F1 [NCBI] 0.000302783
WG [NCBI] 0.000283087
HESX1 [NCBI] 0.000251926
PRL [NCBI] 0.000160644
LHX4 [NCBI] 0.000156938
PROP1 [NCBI] 0.000153784
TRH [NCBI] 8.15049e-05
SOX3 [NCBI] 7.54373e-05
TBX19 [NCBI] 5.34575e-05
LHX3 [NCBI] 5.27244e-05
HES1 [NCBI] 4.28478e-05
PITX1 [NCBI] 3.39464e-05
GH1 [NCBI] 3.18607e-05
SOX2 [NCBI] 2.33504e-05
GHRH [NCBI] 2.12844e-05
IGF1 [NCBI] 2.00191e-05
GLI2 [NCBI] 1.52133e-05
PITX3 [NCBI] 1.40936e-05
TF [NCBI] 1.39334e-05
HSD11B1 [NCBI] 1.37592e-05
GLI3 [NCBI] 1.33728e-05
AVP [NCBI] 1.30292e-05
GHR [NCBI] 1.13791e-05
IGFBP3 [NCBI] 9.39504e-06
SIX6 [NCBI] 9.22387e-06
PHF6 [NCBI] 9.22387e-06
TLE1 [NCBI] 9.05217e-06
CSH1 [NCBI] 8.49884e-06
LPL [NCBI] 8.42012e-06
OTX2 [NCBI] 7.74664e-06
SCG5 [NCBI] 6.30083e-06
IGFBP2 [NCBI] 6.26874e-06
NR0B1 [NCBI] 6.23725e-06
PTH [NCBI] 6.21234e-06
MTPN [NCBI] 6.05975e-06
ARX [NCBI] 6.00452e-06
FGF8 [NCBI] 5.77628e-06
HSD11B2 [NCBI] 5.21746e-06
PLTP [NCBI] 4.96634e-06
EIF4EBP1 [NCBI] 4.85381e-06
AMH [NCBI] 4.64956e-06
TH [NCBI] 4.45503e-06
AQP2 [NCBI] 4.10435e-06
SHH [NCBI] 3.21765e-06
SHBG [NCBI] 2.21817e-06
APOB [NCBI] 2.16346e-06
CCL2 [NCBI] 1.96674e-06
CETP [NCBI] 1.82266e-06
JAK2 [NCBI] 1.72951e-06
PTHLH [NCBI] 1.71465e-06
TG [NCBI] 1.43654e-06
NOS3 [NCBI] 1.07843e-06
EPO [NCBI] 5.04168e-07
APOE [NCBI] 3.17155e-07
CASP3 [NCBI] 2.35974e-07



OMIM


 OMIM Link Information
gain		 01
PHP [NCBI] 0.00621733
pituitary dwarfism iii [NCBI] 0.000659843
septooptic dysplasia [NCBI] 0.000642623
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina [NCBI] 0.000640751
anosmia, congenital [NCBI] 0.000640751
SRS [NCBI] 0.000552479
PRL [NCBI] 0.000499095
POU1F1 [NCBI] 0.000450011
PHS [NCBI] 0.000433242
PROP1 [NCBI] 0.000372299
SPS [NCBI] 0.000302645
thyrotropin deficiency, isolated [NCBI] 0.000247887
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 0.000239379
optic nerve hypoplasia, bilateral [NCBI] 0.000192916
eunuchoidism, familial hypogonadotropic [NCBI] 0.000164976
HESX1 [NCBI] 0.000161561
SOX3 [NCBI] 0.000157233
GHRH [NCBI] 0.000156193
GH1 [NCBI] 0.000142835
IGFALS [NCBI] 0.000128386
CJD [NCBI] 0.000123343
deafness, sensorineural, with pituitary dwarfism [NCBI] 0.000118781
pituitary dwarfism with large sella turcica [NCBI] 0.000118781
rhyns syndrome [NCBI] 0.000118781
hypopituitarism, congenital, with central diabetes insipidus [NCBI] 0.000118781
arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies [NCBI] 0.000118781
MKKS [NCBI] 0.000117928
AVP [NCBI] 0.000116758
KAL1 [NCBI] 0.000101073
arthrogryposis, distal, with mental retardation and characteristic facies [NCBI] 9.63185e-05
CRH [NCBI] 9.05492e-05
langerhans cell histiocytosis [NCBI] 8.23491e-05
NSIAD [NCBI] 8.23491e-05
cleft larynx, posterior [NCBI] 7.50102e-05
chromosome 18p deletion syndrome [NCBI] 7.50102e-05
neural tube defects, x-linked [NCBI] 7.50102e-05
TRS [NCBI] 6.79721e-05
acth deficiency [NCBI] 6.79721e-05
IGF1 [NCBI] 6.78988e-05
SMMCI [NCBI] 5.54634e-05
LHX3 [NCBI] 5.23214e-05
JBS [NCBI] 5.16374e-05
HSS [NCBI] 5.16374e-05
KAL2 [NCBI] 4.97212e-05
RIEG1 [NCBI] 4.91313e-05
SLE [NCBI] 4.54871e-05
TF [NCBI] 4.30073e-05
CES [NCBI] 3.92139e-05
hypogonadotropic hypogonadism [NCBI] 3.17182e-05
PITX2 [NCBI] 2.93437e-05
ARX [NCBI] 2.82608e-05
FA [NCBI] 2.78106e-05
NR0B1 [NCBI] 2.66918e-05
CDLS1 [NCBI] 2.66684e-05
GNRH1 [NCBI] 2.32871e-05
AQP2 [NCBI] 2.31275e-05
STAT5A [NCBI] 2.134e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 1.98474e-05
JAK2 [NCBI] 1.67496e-05
PLTP [NCBI] 1.61895e-05
LPL [NCBI] 1.4701e-05
GHR [NCBI] 1.45539e-05
AMH [NCBI] 1.29446e-05
CVID [NCBI] 1.15817e-05
TH [NCBI] 4.00486e-06
lymphoma, non-hodgkin, familial [NCBI] 2.798e-06
APOB [NCBI] 2.66206e-06
KLK3 [NCBI] 2.49774e-06
SHBG [NCBI] 2.14113e-06
EPO [NCBI] 1.89358e-06
PTH [NCBI] 1.6375e-06
TG [NCBI] 2.12518e-07



Database Center for Life Science