Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Infant Nutrition Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
KCNJ11 [NCBI] 1.50464e-05



OMIM


 OMIM Link Information
gain		 01
trichohepatoenteric syndrome [NCBI] 0.00102023
diarrhea 2, with microvillous atrophy [NCBI] 0.000847142
enterokinase deficiency [NCBI] 0.000230433
edinburgh malformation syndrome [NCBI] 0.000125783
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome [NCBI] 0.000101727
ESX1L [NCBI] 0.000100528
NSHPT [NCBI] 9.11242e-05
EPD [NCBI] 8.76406e-05
GAD1 [NCBI] 8.09985e-05
ALS1 [NCBI] 6.08404e-05
SDS [NCBI] 5.91571e-05
CF [NCBI] 3.77146e-05



Database Center for Life Science