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MeSH keywords -> Related genes, diseases (OMIM)


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01 Pierre Robin Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
TARPS [NCBI] 0.000817003
GER [NCBI] 0.000198305
ESCO2 [NCBI] 1.6933e-05
COL11A1 [NCBI] 1.56767e-05
KCNJ2 [NCBI] 1.34804e-05
COL11A2 [NCBI] 1.22467e-05
SOX9 [NCBI] 1.16181e-05
COL2A1 [NCBI] 1.14692e-05



OMIM


 OMIM Link Information
gain		 01
pierre robin sequence with pectus excavatum and rib and scapular anomalies [NCBI] 0.00270288
TARPS [NCBI] 0.00221606
ear malformation [NCBI] 0.000880362
catel-manzke syndrome [NCBI] 0.000543957
mohr syndrome [NCBI] 0.000533572
pierre robin syndrome [NCBI] 0.000514281
cerebrocostomandibular syndrome [NCBI] 0.00037333
STL1 [NCBI] 0.000305412
arthrogryposis multiplex congenita with whistling face [NCBI] 0.000225178
CPI [NCBI] 0.000196541
pierre robin sequence with facial and digital anomalies [NCBI] 0.000127818
ventricular extrasystoles with syncope, perodactyly, and robin sequence [NCBI] 0.000127818
robin sequence with distinctive facial appearance and brachydactyly [NCBI] 0.000127818
ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum [NCBI] 0.000105351
pierre robin syndrome and oligodactyly [NCBI] 0.000105351
myopathy, congenital nonprogressive, with moebius sequence and robin sequence [NCBI] 9.68753e-05
robin sequence with cleft mandible and limb anomalies [NCBI] 9.13729e-05
COL11A2 [NCBI] 7.32984e-05
WZS [NCBI] 7.07404e-05
WGN1 [NCBI] 6.83453e-05
marshall syndrome [NCBI] 6.72698e-05
OPD2 [NCBI] 6.6262e-05
SOX9 [NCBI] 6.62258e-05
apnea, obstructive sleep [NCBI] 6.61063e-05
campomelic dysplasia [NCBI] 5.10787e-05
phenylketonuria [NCBI] 4.53799e-05
AMC [NCBI] 4.34971e-05
velocardiofacial syndrome [NCBI] 4.32681e-05



Database Center for Life Science