Bilateral multicystic renal dysplasia

disorder

SNOMED 717749002CUI C1840451

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Ureteropelvic junction obstruction

Frequent (30-79%)HP:0000074

Back pain

Occasional (5-29%)HP:0003418

Congenital megaureter

Occasional (5-29%)HP:0008676

Dysplastic kidneys

Occasional (5-29%)HP:0000110

Echogenic kidneys

Occasional (5-29%)HP:0004719

Hydronephrosis

Occasional (5-29%)HP:0000126

Kidney pain

Occasional (5-29%)HP:0030157

Renal failure in adulthood

Occasional (5-29%)HP:0000083

Small kidneys

Occasional (5-29%)HP:0000089

Ureteral dilatation

Occasional (5-29%)HP:0000072

Related Conditions

Multicystic renal dysplasia(parent)

Bilateral renal dysgenesis(parent)

Quick Facts

SNOMED CT: 717749002
UMLS CUI: C1840451
Fully Specified Name: Bilateral multicystic renal dysplasia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.