Primary hyperoxaluria, type II

disorder

SNOMED 40951006CUI C0268165

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.

Elevated urinary L-glycerate level

Always present (100%)HP:6000670

Hyperoxaluria

Very frequent (80-99%)HP:0003159

Kidney stones

Very frequent (80-99%)HP:0000787

Nephrocalcinosis

Very frequent (80-99%)HP:0000121

Calcium oxalate kidney stones

Frequent (30-79%)HP:0008672

Repeated bladder infections

Frequent (30-79%)HP:0000010

Ureteral obstruction

Frequent (30-79%)HP:0006000

Renal insufficiency

Occasional (5-29%)HP:0000083

Abnormal circulating creatinine concentration

Excluded (<1%)HP:0012100

Abnormality of urine Ca2+ concentration

Excluded (<1%)HP:0011280

High urine occult blood

HP:0000790

Metabolic acidosis

Excluded (<1%)HP:0001942

Reduced hepatic glyoxylate reductase activity

HP:6000638

Related Conditions

Primary hyperoxaluria(parent)

Quick Facts

SNOMED CT: 40951006
UMLS CUI: C0268165
Fully Specified Name: Primary hyperoxaluria, type II (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.