Iminoglycinuria

disorder

SNOMED 84121007CUI C0268654

Overview

Iminoglycinuria 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.

Elevated urinary hydroxyproline

Always present (100%)HP:0003080

Hyperglycinuria

Always present (100%)HP:0003108

Proline high in urine

Always present (100%)HP:0003137

Dull intelligence

HP:0001249

Eye disease

HP:0000478

Related Conditions

Neonatal iminoglycinuria(child)

Familial renal iminoglycinuria(child)

Specific renal tubule transport defect(parent)

Amino acid transport disorder(parent)

Metabolic renal disease(parent)

Quick Facts

SNOMED CT: 84121007
UMLS CUI: C0268654
Fully Specified Name: Iminoglycinuria (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.