Congenital nephrosis, cerebral ventriculomegaly syndrome

disorder

SNOMED 1216942009CUI C1857423

Overview

Congenital nephrosis, cerebral ventriculomegaly syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Seizures

Always present (100%)HP:0001250

Corticomedullary renal cysts

Frequent (30-79%)HP:0000108

Dilated cerebral ventricle

Frequent (30-79%)HP:0002119

Echogenic kidneys

Frequent (30-79%)HP:0004719

Fetal pericardial effusion

Occasional (5-29%)HP:0025671

Heterotopias

Occasional (5-29%)HP:0002282

Premature birth

Occasional (5-29%)HP:0001622

Tubular luminal dilatation

Occasional (5-29%)HP:0032622

VSD

Occasional (5-29%)HP:0001629

Increased amniotic fluid index

HP:0001561

Nonsyndromal hydrocephalus

HP:0000238

Postaxial hexadactyly

HP:0100259

Renal failure in adulthood

HP:0000083

Wider than typical opening or gap

HP:0002617

Related Conditions

Congenital enlargement of ventricle of brain(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Hereditary nephropathy(parent)

Congenital cystic kidney disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1216942009
UMLS CUI: C1857423
Fully Specified Name: Cerebral ventriculomegaly, cystic kidney disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.