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01 Hydronephrosis [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.00458619
PUJO [NCBI] 0.000230282
UMOD [NCBI] 2.90889e-05
EGF [NCBI] 2.50131e-05
ID2 [NCBI] 1.80422e-05
PTGES2 [NCBI] 1.50015e-05
AQP2 [NCBI] 1.49837e-05
AMBP [NCBI] 1.35349e-05
GAPDH [NCBI] 1.29523e-05
CDC5L [NCBI] 1.23852e-05
PHLDA1 [NCBI] 1.20977e-05
COL9A3 [NCBI] 9.89069e-06
DLG1 [NCBI] 9.75058e-06
ADAMTS1 [NCBI] 8.95737e-06
CCL1 [NCBI] 8.91556e-06
NFKB2 [NCBI] 8.87476e-06
AVP [NCBI] 8.49547e-06
AGTR2 [NCBI] 8.24178e-06
PTGER1 [NCBI] 7.35144e-06
TGFB1 [NCBI] 7.00005e-06
EPO [NCBI] 6.64458e-06
SELPLG [NCBI] 5.96522e-06
ADM [NCBI] 5.92216e-06
SHH [NCBI] 5.36657e-06
AHR [NCBI] 5.3067e-06
TGFBR1 [NCBI] 5.15238e-06
ALK [NCBI] 5.13021e-06
EGFR [NCBI] 4.86719e-06
AGT [NCBI] 4.47122e-06
CCL2 [NCBI] 4.02364e-06
ACE [NCBI] 3.4283e-06
SOD1 [NCBI] 3.34939e-06
TH [NCBI] 3.16762e-06
NPY [NCBI] 2.80754e-06
VWF [NCBI] 2.28242e-06
AFP [NCBI] 2.15326e-06
PTH [NCBI] 1.41119e-06



OMIM


 OMIM Link Information
gain		 01
MRD [NCBI] 0.0100727
schinzel-giedion midface-retraction syndrome [NCBI] 0.00486215
genitopatellar syndrome [NCBI] 0.000579249
UFS [NCBI] 0.000482774
kyphomelic dysplasia [NCBI] 0.000408926
megacystis-microcolon-intestinal hypoperistalsis syndrome [NCBI] 0.000370626
megaduodenum and/or megacystis [NCBI] 0.000340301
VUR1 [NCBI] 0.000281437
noduli cutanei, multiple, with urinary tract abnormalities [NCBI] 0.000257125
hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation [NCBI] 0.000257125
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 0.000252213
holoprosencephaly [NCBI] 0.000235958
ureterocele [NCBI] 0.000226176
CDC5L [NCBI] 0.000151073
AQP2 [NCBI] 0.000143518
MKKS [NCBI] 0.000137076
USF2 [NCBI] 0.000128432
WFS1 [NCBI] 0.000124011
OFD7 [NCBI] 0.000105843
mental retardation with epilepsy and characteristic facies [NCBI] 9.18637e-05
TBX18 [NCBI] 8.48492e-05
weyers ulnar ray/oligodactyly syndrome [NCBI] 8.45153e-05
whistling face syndrome, recessive form [NCBI] 7.7463e-05
CPI [NCBI] 7.62129e-05
EGF [NCBI] 7.01716e-05
PGL4 [NCBI] 6.99871e-05
HPE3 [NCBI] 6.88341e-05
xanthinuria, type i [NCBI] 6.77584e-05
diabetes insipidus, nephrogenic, autosomal [NCBI] 6.58021e-05
SLC12A1 [NCBI] 6.24949e-05
DLG1 [NCBI] 6.24949e-05
JK [NCBI] 6.24949e-05
diabetes insipidus, nephrogenic, x-linked [NCBI] 5.79589e-05
AQP3 [NCBI] 5.63228e-05
mucopolysaccharidosis type vii [NCBI] 5.5853e-05
PHS [NCBI] 5.11911e-05
GAPDH [NCBI] 4.9385e-05
AVSD [NCBI] 4.06664e-05
AQP1 [NCBI] 3.97744e-05
ACH [NCBI] 3.51233e-05
NPPA [NCBI] 3.09348e-05
GUSB [NCBI] 3.01875e-05
ADM [NCBI] 2.48545e-05
BWS [NCBI] 2.07057e-05
AVP [NCBI] 1.87644e-05
AHR [NCBI] 1.86753e-05
EPO [NCBI] 1.46242e-05
PTHLH [NCBI] 1.40102e-05
EGFR [NCBI] 8.79538e-06
TH [NCBI] 6.24868e-06
NPY [NCBI] 4.82965e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.09581e-06
AFP [NCBI] 2.33058e-06
SLE [NCBI] 2.3086e-06
CRC [NCBI] 7.91507e-07
PTH [NCBI] 3.21473e-07



Database Center for Life Science