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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anus, Imperforate [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.00043676
CDAGS [NCBI] 0.000389986
HMI [NCBI] 0.000291438
AFA [NCBI] 0.000252459
SALL1 [NCBI] 0.000144243
GLI3 [NCBI] 7.05912e-05
T [NCBI] 2.2027e-05
CECR1 [NCBI] 1.45183e-05
MKS1 [NCBI] 1.22155e-05
IL17RA [NCBI] 1.02701e-05
HOXD13 [NCBI] 9.21733e-06
IRF6 [NCBI] 8.82547e-06
TWIST1 [NCBI] 7.41137e-06
BID [NCBI] 6.88108e-06
CKAP4 [NCBI] 6.4099e-06
SHH [NCBI] 6.12669e-06
TP63 [NCBI] 5.68441e-06
ACHE [NCBI] 3.85788e-06
AFP [NCBI] 2.85024e-06



OMIM


 OMIM Link Information
gain		 01
CES [NCBI] 0.00140297
TBS [NCBI] 0.00129976
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000930625
cdags syndrome [NCBI] 0.000900049
anorectal anomalies [NCBI] 0.000900049
HFM [NCBI] 0.000795904
exstrophy of bladder [NCBI] 0.000724991
oeis complex [NCBI] 0.000603463
PHS [NCBI] 0.000565705
ACC [NCBI] 0.000521852
OKS [NCBI] 0.000433364
vater association [NCBI] 0.000333365
SALL1 [NCBI] 0.000294842
JBS [NCBI] 0.000275154
anus, imperforate [NCBI] 0.000224694
anus, imperforate [NCBI] 0.000224694
spondylocostal dysostosis with anal atresia and urogenital anomalies [NCBI] 0.000193755
anal atresia, hypospadias, and penoscrotal inversion [NCBI] 0.00017978
cleft larynx, posterior [NCBI] 0.000162847
vacterl association with hydrocephalus, x-linked [NCBI] 0.000147522
FANCB [NCBI] 0.000142221
GLI3 [NCBI] 0.000115434
hair whorl [NCBI] 0.000112254
aphalangy with hemivertebrae [NCBI] 0.000112254
growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia [NCBI] 0.000112254
polydactyly, imperforate anus, and vertebral anomalies [NCBI] 0.000112254
cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction [NCBI] 0.000112254
GCPS [NCBI] 9.27342e-05
CECR1 [NCBI] 9.15682e-05
dk phocomelia syndrome [NCBI] 8.97971e-05
stratton-parker syndrome [NCBI] 8.97971e-05
thymic-renal-anal-lung dysplasia [NCBI] 8.97971e-05
omphalocele, diaphragmatic hernia, and radial ray defects [NCBI] 8.13307e-05
ivic syndrome [NCBI] 7.58383e-05
GLI2 [NCBI] 6.9211e-05
SMOH [NCBI] 6.9211e-05
vacterl association with hydrocephalus [NCBI] 6.35035e-05
tracheoesophageal fistula with or without esophageal atresia [NCBI] 6.35035e-05
polydactyly, postaxial, type a1 [NCBI] 6.35035e-05
T [NCBI] 6.3036e-05
GLI [NCBI] 6.3036e-05
currarino syndrome [NCBI] 5.40619e-05
feingold syndrome [NCBI] 5.29189e-05
PTCH1 [NCBI] 5.11499e-05
waardenburg-shah syndrome [NCBI] 4.9917e-05
NR5A1 [NCBI] 4.94573e-05
UMS [NCBI] 4.81941e-05
ABS [NCBI] 4.16409e-05
MKKS [NCBI] 4.11163e-05
fraser syndrome [NCBI] 4.06092e-05
MTTL1 [NCBI] 3.80819e-05
charge syndrome [NCBI] 3.78777e-05
CMTC [NCBI] 3.48698e-05
hypogonadotropic hypogonadism [NCBI] 2.56305e-05
SHH [NCBI] 2.43406e-05
ACHE [NCBI] 1.16939e-05
AFP [NCBI] 6.79479e-06
FA [NCBI] 2.15492e-06



Database Center for Life Science