Cystinuria, type 1

disorder

SNOMED 37183000CUI C0268643

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Hypotonia cystinuria syndrome(child)

Atypical hypotonia cystinuria syndrome(child)

2p21 microdeletion syndrome(child)

Cystinuria(parent)

Disease of skeletal muscle(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary nephropathy(parent)

Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT: 37183000
UMLS CUI: C0268643
Fully Specified Name: Cystinuria, type 1 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.