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MeSH keywords -> Related genes, diseases (OMIM)


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01 Diabetes Insipidus [NCBI]


Gene


Gene Link Information
Gain
01
AVP [NCBI] 0.00107156
AQP2 [NCBI] 0.000218515
AVPR2 [NCBI] 0.000154636
AQP3 [NCBI] 1.72139e-05
EVI1 [NCBI] 1.14582e-05
TRH [NCBI] 9.12959e-06
PTH [NCBI] 8.74681e-06
AQP1 [NCBI] 6.15055e-06
SCG5 [NCBI] 6.15055e-06
OCRL [NCBI] 6.05613e-06
PAM [NCBI] 5.32419e-06
PTHLH [NCBI] 5.26991e-06
AQP4 [NCBI] 5.10271e-06
CCK [NCBI] 4.63655e-06
SLC9A3 [NCBI] 4.25772e-06
VWF [NCBI] 2.57373e-06
CTSL1 [NCBI] 2.41748e-06
PRL [NCBI] 2.08621e-06
PTEN [NCBI] 9.05827e-07
AFP [NCBI] 3.84049e-07
CFTR [NCBI] 1.77613e-07




OMIM


OMIM Link Information
gain
01
AVP [NCBI] 0.00671529
diabetes insipidus, nephrogenic, x-linked [NCBI] 0.00216516
diabetes insipidus, neurohypophyseal type [NCBI] 0.00191741
WFS1 [NCBI] 0.00136935
diabetes insipidus, nephrogenic, autosomal [NCBI] 0.00107114
AVPR2 [NCBI] 0.000868917
proteus syndrome [NCBI] 0.000830911
AQP2 [NCBI] 0.000253376
diabetes insipidus, neurohypophyseal type [NCBI] 0.000228234
septooptic dysplasia [NCBI] 0.000126673
hypopituitarism, congenital, with central diabetes insipidus [NCBI] 0.000114013
diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification [NCBI] 0.000114013
autonomic control, congenital failure of [NCBI] 0.000107379
langerhans cell histiocytosis [NCBI] 7.75929e-05
optic nerve hypoplasia, bilateral [NCBI] 7.75929e-05
SLE [NCBI] 7.74449e-05
pseudopapilledema [NCBI] 7.35111e-05
bartter syndrome, antenatal, type 1 [NCBI] 7.02613e-05
bartter syndrome, antenatal, type 2 [NCBI] 5.35882e-05
SLSN1 [NCBI] 4.76449e-05
ALMS [NCBI] 4.50489e-05
OXT [NCBI] 4.27692e-05
AQP3 [NCBI] 3.60626e-05
BRRS [NCBI] 3.24057e-05
NPPA [NCBI] 2.96968e-05
SLC12A3 [NCBI] 2.69448e-05
AKR1B1 [NCBI] 2.46713e-05
AQP1 [NCBI] 1.98829e-05
PTGS2 [NCBI] 1.41152e-05
AFP [NCBI] 1.29357e-05
von willebrand disease [NCBI] 8.54823e-06
PRL [NCBI] 6.83612e-06
hemophilia a [NCBI] 6.36295e-06
CRH [NCBI] 5.94763e-06
GNRH1 [NCBI] 1.75842e-06
PTH [NCBI] 6.89432e-07
CCK [NCBI] 3.31313e-07
thrombocytopenic purpura, autoimmune [NCBI] 4.81837e-08




Database Center for Life Science