|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Megacystis microcolon intestinal hypoperistalsis syndrome from the curated CTD Gene-Disease Associations dataset.
|ACTG2||actin, gamma 2, smooth muscle, enteric||2.88009|