Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 De Lange Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
NIPBL [NCBI] 0.000368928
GER [NCBI] 0.000317425
SMC1A [NCBI] 4.13084e-05
NAALADL2 [NCBI] 1.78633e-05
CHRD [NCBI] 1.45844e-05
GSC [NCBI] 1.29339e-05
ESCO2 [NCBI] 1.29339e-05
SMC3 [NCBI] 1.19533e-05
TNKS [NCBI] 1.05861e-05
H2AFX [NCBI] 5.92765e-06



OMIM


 OMIM Link Information
gain		 01
CDLS1 [NCBI] 0.0113402
coffin-siris syndrome [NCBI] 0.00154489
cerebrofaciothoracic dysplasia [NCBI] 0.000991404
NIPBL [NCBI] 0.000664756
SMC1A [NCBI] 0.000185323
CHRD [NCBI] 0.000157763
brachmann-de lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay [NCBI] 0.0001105
CDLS3 [NCBI] 0.0001105
CDLS2 [NCBI] 0.0001105
n-acetylated alpha-linked acidic dipeptidase-like 2 [NCBI] 9.22788e-05
SMC3 [NCBI] 7.8499e-05
GSC [NCBI] 6.54099e-05
PAPPA [NCBI] 6.23221e-05
AGTR1 [NCBI] 5.18591e-05
RBS [NCBI] 3.6191e-05



Database Center for Life Science