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Megacystis, microcolon, hypoperistalsis syndrome
disorderSNOMED 253781004CUI C1608393
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Belly bloating
Very frequent (80-99%)HP:0003270
Intestinal hypoperistalsis
Very frequent (80-99%)HP:0100771
Megacystis
Very frequent (80-99%)HP:0000021
Microcolon
Very frequent (80-99%)HP:0004388
Nausea and vomiting
Very frequent (80-99%)HP:0002017
Digestive system disease
Frequent (30-79%)HP:0011024
Increased amniotic fluid index
Frequent (30-79%)HP:0001561
Intestinal malrotation
Frequent (30-79%)HP:0002566
Multicystic kidney dysplasia
Frequent (30-79%)HP:0000003
Uroureter
Frequent (30-79%)HP:0000072
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Cryptorchidism
Occasional (5-29%)HP:0000028
Heart tumor
Occasional (5-29%)HP:0100544
Infection in blood stream
Occasional (5-29%)HP:0100806
Omphalocoele
Occasional (5-29%)HP:0001539
Umbilical hernia
Occasional (5-29%)HP:0001537
Fetal megacystis
HP:0010956
Generalised oedema
HP:0007430
Oligohydramnios
HP:0001562
Related Conditions
Congenital functional disorders of the colon(parent)
Motility disorder of large intestine(parent)
Congenital anomaly of large intestine(parent)
Hereditary disorder of the urinary system(parent)
Multiple system malformation syndrome(parent)
Autosomal hereditary disorder(parent)
Digestive system hereditary disorder(parent)
Congenital dilatation of bladder(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 253781004
- UMLS CUI
- C1608393
- Fully Specified Name
- Megacystis, microcolon, hypoperistalsis syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 19
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.