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01 Anal Canal [NCBI]


Gene


Gene Link Information
Gain
01
FGS2 [NCBI] 0.000442596
MS [NCBI] 0.000305475
MNX1 [NCBI] 0.000111572
VIP [NCBI] 2.80047e-05
SALL1 [NCBI] 2.62495e-05
ACHE [NCBI] 1.54003e-05
SHH [NCBI] 1.14709e-05
FGF10 [NCBI] 9.87726e-06
GLI3 [NCBI] 9.40524e-06
KRT7 [NCBI] 8.19553e-06
CKAP4 [NCBI] 8.18739e-06
FAM58A [NCBI] 7.98459e-06
KRT20 [NCBI] 7.92172e-06
CHGA [NCBI] 7.89352e-06
LHFPL5 [NCBI] 7.64439e-06
TP63 [NCBI] 7.14523e-06
TAOK1 [NCBI] 6.15169e-06
PCSK1 [NCBI] 5.61511e-06
HIC1 [NCBI] 5.295e-06
SRPK1 [NCBI] 5.295e-06
HOXD13 [NCBI] 5.05303e-06
CADM1 [NCBI] 4.80683e-06
GLI2 [NCBI] 4.77383e-06
EDNRB [NCBI] 4.72629e-06
CD68 [NCBI] 4.70157e-06
CDH15 [NCBI] 4.69581e-06
EWSR1 [NCBI] 4.68091e-06
AR [NCBI] 3.72218e-06
APOD [NCBI] 3.62764e-06
DLX3 [NCBI] 3.48994e-06
RASSF1 [NCBI] 3.46372e-06
INPP5D [NCBI] 3.21397e-06
MYOD1 [NCBI] 3.16198e-06
ADCYAP1 [NCBI] 3.13392e-06
MUC2 [NCBI] 3.00733e-06
ENG [NCBI] 2.90026e-06
CDKN1B [NCBI] 2.89066e-06
IL1B [NCBI] 2.80176e-06
OPRL1 [NCBI] 2.68318e-06
MLH1 [NCBI] 2.67362e-06
PYY [NCBI] 2.64364e-06
BMP4 [NCBI] 2.5864e-06
CTGF [NCBI] 2.21218e-06
FOXP3 [NCBI] 2.16794e-06
TRH [NCBI] 1.41762e-06
MPO [NCBI] 1.21024e-06
TGFB1 [NCBI] 1.20952e-06
PCNA [NCBI] 1.1165e-06
NPY [NCBI] 7.31937e-07




OMIM


OMIM Link Information
gain
01
anorectal anomalies [NCBI] 0.00425954
cdags syndrome [NCBI] 0.00109002
currarino syndrome [NCBI] 0.00106119
kabuki syndrome [NCBI] 0.00102107
FGS2 [NCBI] 0.00097306
APC [NCBI] 0.000918797
TBS [NCBI] 0.000853583
OSCS [NCBI] 0.000796235
corpus callosum, agenesis of, with facial anomalies and robin sequence [NCBI] 0.000759091
intestinal atresia, multiple [NCBI] 0.000653047
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000582277
dubowitz syndrome [NCBI] 0.000582277
sacral defect with anterior meningocele [NCBI] 0.000498208
CES [NCBI] 0.000466061
HFM [NCBI] 0.000302057
MKKS [NCBI] 0.000190173
anus, imperforate [NCBI] 0.000189459
anal sphincter myopathy, internal [NCBI] 0.000189459
ASDP [NCBI] 0.000189459
cholesterol pneumonia [NCBI] 0.000189459
MOTA [NCBI] 0.000189459
syndactyly with renal and anogenital malformations [NCBI] 0.000189459
anus, imperforate [NCBI] 0.000189459
BGS [NCBI] 0.000182705
HLXB9 [NCBI] 0.000143633
SALL1 [NCBI] 0.000134319
rapadilino syndrome [NCBI] 0.000125835
vacterl association with hydrocephalus [NCBI] 0.000125835
hypotension, orthostatic [NCBI] 0.000125835
arhinia, choanal atresia, and microphthalmia [NCBI] 0.000125835
VIP [NCBI] 0.000120044
acrorenal-mandibular syndrome [NCBI] 0.000118711
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 0.000113041
vater association [NCBI] 9.76705e-05
DRRS [NCBI] 8.78482e-05
SHH [NCBI] 8.72139e-05
NETH [NCBI] 8.58578e-05
ABS [NCBI] 8.06333e-05
OKS [NCBI] 7.13439e-05
RIEG1 [NCBI] 6.8176e-05
PHS [NCBI] 6.62569e-05
LSA [NCBI] 6.27944e-05
ACHE [NCBI] 5.7323e-05
AVSD [NCBI] 5.17621e-05
TAOK1 [NCBI] 4.76917e-05
velocardiofacial syndrome [NCBI] 4.45258e-05
BBS [NCBI] 3.96044e-05
SALL4 [NCBI] 3.66677e-05
OPMD [NCBI] 3.40201e-05
PIAS1 [NCBI] 3.12374e-05
FGF10 [NCBI] 2.81898e-05
MTTL1 [NCBI] 2.62071e-05
GIST [NCBI] 2.41849e-05
DGS [NCBI] 2.19034e-05
BMP4 [NCBI] 2.00768e-05
lymphoma, non-hodgkin, familial [NCBI] 1.44752e-05
AR [NCBI] 1.13752e-05
CTGF [NCBI] 9.98655e-06
PYY [NCBI] 9.94898e-06
NPPA [NCBI] 3.69044e-06
MPO [NCBI] 1.5409e-06
PCNA [NCBI] 1.24234e-06
VEGF [NCBI] 9.2424e-07
NPY [NCBI] 7.97726e-08




Database Center for Life Science