Ileitis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An inflammatory bowel disease characterized by inflammation located_in ileum, has_symptom diarrhea, has_symptom abdominal pain, often in the right lower quadrant, has_symptom weight loss. (Human Disease Ontology, DOID_0060189)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007079
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Genes

1 genes/proteins associated with the disease Ileitis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit) 2.88009