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MeSH keywords -> Related genes, diseases (OMIM)


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01 Choanal Atresia [NCBI]


Gene


Gene Link Information
Gain
01
GER [NCBI] 0.000317425
CHD7 [NCBI] 0.000126613
SHH [NCBI] 2.71262e-05
CDH7 [NCBI] 1.54394e-05
MMP23B [NCBI] 1.54394e-05
SEMA3E [NCBI] 1.35427e-05
FOXE1 [NCBI] 1.11906e-05
FGFR3 [NCBI] 6.38454e-06




OMIM


OMIM Link Information
gain
01
PCA [NCBI] 0.00782859
oculootofacial dysplasia [NCBI] 0.00206288
burn-mckeown syndrome [NCBI] 0.00206288
charge syndrome [NCBI] 0.00203562
ACC [NCBI] 0.000431005
coffin-siris syndrome [NCBI] 0.000358734
holoprosencephaly [NCBI] 0.000323443
EEC1 [NCBI] 0.000319041
CHD7 [NCBI] 0.000257554
carbimazole sensitivity [NCBI] 0.000216521
hypothyroidism, athyroidal, with spiky hair and cleft palate [NCBI] 0.000206921
SEMA3E [NCBI] 0.000178697
radial ray hypoplasia with choanal atresia [NCBI] 0.000130439
breasts and nipples, absence of [NCBI] 0.000107971
monosomy 9p syndrome [NCBI] 9.39907e-05
charge-like syndrome, x-linked [NCBI] 9.39907e-05
SMMCI [NCBI] 6.7023e-05
FOXE1 [NCBI] 6.58157e-05
PPS [NCBI] 6.24992e-05
KAL2 [NCBI] 6.12371e-05
CHNG2 [NCBI] 5.89784e-05
PITX2 [NCBI] 5.60041e-05
PHS [NCBI] 5.3289e-05
SHH [NCBI] 3.07419e-05
PWS [NCBI] 1.19524e-05




Database Center for Life Science