Oligomeganephronic hypoplasia of kidney

disorder

SNOMED 18417009CUI C0431694

Overview

Oligomeganephronic hypoplasia of kidney 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.

Abnormal nephron morphology

Very frequent (80-99%)HP:0012575

Bilateral renal hypoplasia

Very frequent (80-99%)HP:0012584

Decreased glomerular filtration rate

Very frequent (80-99%)HP:0012213

Decreased numbers of glomeruli

Very frequent (80-99%)HP:0005563

Glomeruli enlarged

Very frequent (80-99%)HP:0030162

Increased creatinine

Very frequent (80-99%)HP:0003259

Proteinuria

Very frequent (80-99%)HP:0000093

Renal failure

Very frequent (80-99%)HP:0000083

Abnormality of medullary pyramid morphology

Frequent (30-79%)HP:0025361

Abnormality of renal cortex morphology

Frequent (30-79%)HP:0011035

Birth weight less than 10th percentile

Frequent (30-79%)HP:0001518

End-stage renal disease

Frequent (30-79%)HP:0003774

Premature birth

Frequent (30-79%)HP:0001622

Renal tubular cell atrophy

Frequent (30-79%)HP:0000092

Dehydration

Occasional (5-29%)HP:0001944

Extreme thirst

Occasional (5-29%)HP:0001959

Branchial cleft cyst

Very rare (1-4%)HP:0009796

Deafness

Very rare (1-4%)HP:0000365

Diaphragmatic hernia

Very rare (1-4%)HP:0000776

Disorder of face

Very rare (1-4%)HP:0000271

Dysmelia

Very rare (1-4%)HP:0040064

Epilepsy

Very rare (1-4%)HP:0001250

High blood pressure

Very rare (1-4%)HP:0000822

Hypoplastic mandible condyle

Very rare (1-4%)HP:0000347

Neurodevelopmental delay

Very rare (1-4%)HP:0012758

Optic disc coloboma

Very rare (1-4%)HP:0000588

Patent ostium secundum

Very rare (1-4%)HP:0001684

Poorly developed lungs

Very rare (1-4%)HP:0002089

Pulmonary venoocclusive disease

Very rare (1-4%)HP:0006518

Unilateral renal agenesis

Very rare (1-4%)HP:0000122

Related Conditions

Congenital hypoplasia of kidney(parent)

Abnormality of nephron morphology(parent)

Quick Facts

SNOMED CT: 18417009
UMLS CUI: C0431694
Fully Specified Name: Oligomeganephronic hypoplasia of kidney (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.