A disease that has its basis in the disruption of intestinal motility.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Chronic intestinal pseudoobstruction | MONDO:0017574 | 5 | |
| Megacystis-microcolon-intestinal hypoperistalsis syndrome | MONDO:0025986 | 5 | |
| Waardenburg-Shah syndrome | MONDO:0019518 | 3 | |
| Familial visceral myopathy | MONDO:0016829 | 2 | |
| Multisystemic smooth muscle dysfunction syndrome | MONDO:0013452 | 2 | ACTA2 |
| Goldberg-Shprintzen syndrome | MONDO:0012280 | KIFBP | |
| Haddad syndrome | MONDO:0020493 | ||
| Hirschsprung disease | MONDO:0018309 | ||
| Hirschsprung disease-ganglioneuroblastoma syndrome | MONDO:0013082 | ||
| Hirschsprung disease-hearing loss-polydactyly syndrome | MONDO:0009342 | ||
| Hirschsprung disease-nail hypoplasia-dysmorphism syndrome | MONDO:0009344 | ||
| Hirschsprung disease-type D brachydactyly syndrome | MONDO:0016294 | ||
| Congenital diarrhea 6 | MONDO:0013825 | GUCY2C | |
| Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency | MONDO:0013843 | GUCY2C | |
| Oculogastrointestinal muscular dystrophy | MONDO:0010181 |
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