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
Belly bloating
Frequent (30-79%)HP:0003270
Premature birth
Frequent (30-79%)HP:0001622
Cryptorchidism
Occasional (5-29%)HP:0000028
Enlarged kidney
Occasional (5-29%)HP:0000105
Oligohydramnios
Occasional (5-29%)HP:0001562
Single kidney
Occasional (5-29%)HP:0000122
VUR
Occasional (5-29%)HP:0000076
High blood pressure
Very rare (1-4%)HP:0000822
Horseshoe kidney
Very rare (1-4%)HP:0000085
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
Related Conditions
Medullary sponge kidney(child)
Polycystic kidney disease, infantile type(child)
Microcystic renal disease(child)
Solitary multilocular renal cyst(child)
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome(child)
Renal hepatic pancreatic dysplasia(child)
Autosomal dominant polycystic kidney disease(child)
Meckel syndrome type 7(child)
Hepatic fibrosis, renal cyst, intellectual disability syndrome(child)
Congenital nephrosis, cerebral ventriculomegaly syndrome(child)
Congenital renal cyst(parent)
Quick Facts
- SNOMED CT
- 82525005
- UMLS CUI
- C0022680
- Fully Specified Name
- Congenital cystic kidney disease (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.