| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
