Megacystis microcolon intestinal hypoperistalsis syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital disease characterized by massive abdominal distension caused by a largely dilated non-obstructed urinary bladder, microcolon and decreased or absent intestinal peristalsis. (Orphanet Rare Disease Ontology, Orphanet_2241)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536138
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Genes

1 genes/proteins associated with the disease Megacystis microcolon intestinal hypoperistalsis syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ACTG2 actin, gamma 2, smooth muscle, enteric 2.88009