MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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