cecal atresia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description congenital blockage or absence of the lumen of the cecum (Mammalian Phenotype Ontology, MP_0009510)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009510
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Genes

2 gene mutations causing the cecal atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2