megacystis-microcolon-intestinal hypoperistalsis syndrome 5
MONDO:0030329Mondo
Findings
No curated finding names megacystis-microcolon-intestinal hypoperistalsis syndrome 5 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset · Fetal onset
HPO, annotations 2026-09-02
Features
8 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Intestinal malrotationHPOHP:0002566
- 2 of 2 reported patients
- MegacystisHPOHP:0000021
- 2 of 2 reported patients
- MicrocolonHPOHP:0004388
- 2 of 2 reported patients
- Hepatic failureHPOHP:0001399
- 1 of 2 reported patients
- HydronephrosisHPOHP:0000126
- 1 of 2 reported patients
- HydroureterHPOHP:0000072
- 1 of 2 reported patients
- OligohydramniosHPOHP:0001562
- 1 of 2 reported patients · Fetal onset
- Portal hypertensionHPOHP:0001409
- 1 of 2 reported patients
Where it sits
Other names
1 name
Resolves to: megacystis-microcolon-intestinal hypoperistalsis syndrome 5
- Also called
- MMIHS5