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Periodic hyperlysinaemia

disorder
SNOMED 341536001CUI C0268555

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.

Dibasicaminoaciduria
HP:0003168
Growth failure
HP:0001510
High blood ammonia levels
HP:0001987
Hyperlysinemia
HP:0002161
Intestinal malabsorption
HP:0002024
Lysinuria
HP:0003297
Mental deficiency
HP:0001249
Torpor
HP:0001254
Trance
HP:0001259

Related Conditions

Quick Facts

SNOMED CT
341536001
UMLS CUI
C0268555
Fully Specified Name
Periodic hyperlysinemia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
9
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.

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