Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Multicystic kidney dysplasia
Very frequent (80-99%)HP:0000003
Respiratory distress, neonatal
Very frequent (80-99%)HP:0002643
Abdominal mass
Frequent (30-79%)HP:0031500
Abdominal swelling
Frequent (30-79%)HP:0003270
Premature birth
Frequent (30-79%)HP:0001622
Cryptorchidism
Occasional (5-29%)HP:0000028
Decreased amniotic fluid index
Occasional (5-29%)HP:0001562
Enlarged kidney
Occasional (5-29%)HP:0000105
Single kidney
Occasional (5-29%)HP:0000122
VUR
Occasional (5-29%)HP:0000076
Fused kidneys
Very rare (1-4%)HP:0000085
High blood pressure
Very rare (1-4%)HP:0000822
Ureterocele
Very rare (1-4%)HP:0000070
Ureteropelvic junction obstruction
Very rare (1-4%)HP:0000074
Ureterovesical junction obstruction
Very rare (1-4%)HP:0030735
Quick Facts
- SNOMED CT
- 737562008
- UMLS CUI
- C3714581
- Fully Specified Name
- Multicystic renal dysplasia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.