Hypervalinemia

disorder

SNOMED 47719001CUI C0268573

Overview

Hypervalinemia 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.

Hyperkinetic movements

HP:0002487

Hypervalinemia

HP:0010910

Increased valine in urine

HP:0033088

Muscle weakness

HP:0001324

Poor weight gain

HP:0001508

Sleepy

HP:0002329

Vomiting

HP:0002013

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Enzymopathy(parent)

Aminoacidemia(parent)

Inborn error of metabolism(parent)

Disorder of valine metabolism(parent)

Quick Facts

SNOMED CT: 47719001
UMLS CUI: C0268573
Fully Specified Name: Hypervalinemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.