Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Fetal Movement [NCBI]

Gene


 Gene Link Information
Gain		 01
TRH [NCBI] 5.03363e-06
AVP [NCBI] 4.62495e-06
PIH [NCBI] 2.83485e-06
TNF [NCBI] 1.36432e-06



OMIM


 OMIM Link Information
gain		 01
pena-shokeir syndrome, type i [NCBI] 0.00855446
lethal congenital contracture syndrome 1 [NCBI] 0.000780625
NLS [NCBI] 0.000513354
holoprosencephaly with fetal akinesia/hypokinesia sequence [NCBI] 0.000360198
encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia [NCBI] 0.000178984
NEM3 [NCBI] 9.49266e-05
SJS1 [NCBI] 8.80934e-05
AMC [NCBI] 8.08978e-05
dystrophia myotonica 1 [NCBI] 5.19339e-05
AVP [NCBI] 3.93632e-05
TS [NCBI] 3.90565e-05
PWS [NCBI] 3.10329e-05
TNF [NCBI] 8.5311e-06
SLE [NCBI] 3.42356e-10



Database Center for Life Science