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MeSH keywords -> Related genes, diseases (OMIM)


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01 Pulmonary Valve Stenosis [NCBI]


Gene


Gene Link Information
Gain
01
FRA12A [NCBI] 0.000499621
PTPN11 [NCBI] 3.98883e-05
GATA4 [NCBI] 2.38313e-05
NKX2-5 [NCBI] 2.15563e-05
JAG1 [NCBI] 1.91603e-05
CRELD1 [NCBI] 1.3697e-05
INVS [NCBI] 1.20249e-05
NFATC1 [NCBI] 1.13417e-05
NF1 [NCBI] 8.85815e-06
MGP [NCBI] 8.63311e-06
BMP2 [NCBI] 6.52285e-06
MTHFR [NCBI] 5.0703e-06




OMIM


OMIM Link Information
gain
01
SVAS [NCBI] 0.00127301
AOS [NCBI] 0.0011114
splenic hypoplasia [NCBI] 0.000773718
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000601472
pulmonic stenosis [NCBI] 0.000595323
cayler cardiofacial syndrome [NCBI] 0.000528971
MVP [NCBI] 0.000464945
leopard syndrome 1 [NCBI] 0.000373565
NS1 [NCBI] 0.000350256
WBS [NCBI] 0.000346037
watson syndrome [NCBI] 0.000288959
keutel syndrome [NCBI] 0.000278895
ALGS1 [NCBI] 0.000156283
AVSD [NCBI] 0.000146808
pulmonic stenosis and congenital nephrosis [NCBI] 0.000118506
disproportionate short stature with ptosis and valvular heart lesions [NCBI] 0.000118506
prune belly syndrome with pulmonic stenosis, mental retardation, and deafness [NCBI] 0.000118506
cranioacrofacial syndrome [NCBI] 0.000118506
pulmonic stenosis and deafness [NCBI] 0.000118506
cardiofaciocutaneous syndrome [NCBI] 0.000108155
NF1 [NCBI] 8.79231e-05
mental retardation, fra12a type [NCBI] 7.47363e-05
VLDLRCH [NCBI] 6.76988e-05
noonan-like/multiple giant cell lesion syndrome [NCBI] 6.42916e-05
PTPN11 [NCBI] 6.27854e-05
BMP2 [NCBI] 6.14875e-05
ATS [NCBI] 6.14849e-05
asplenia with cardiovascular anomalies [NCBI] 5.4349e-05
NPHS1 [NCBI] 5.13668e-05
SGBS1 [NCBI] 4.57264e-05
charge syndrome [NCBI] 4.39408e-05
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 3.5682e-05
NPPA [NCBI] 2.61937e-05
CMH [NCBI] 2.25332e-05




Database Center for Life Science