Related Conditions
Cystinosis(child)
Lysinuric protein intolerance(child)
Neonatal cystine-lysinuria(child)
Fanconi syndrome(child)
Histidine transport defect(child)
Lowe syndrome(child)
Neutral 1 amino acid transport defect(child)
Iminoglycinuria(child)
Cystinuria(child)
Cystinemia(child)
Dicarboxylic aminoaciduria syndrome(child)
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome(child)
Metabolic disorder of transport(parent)
Disorder of amino acid and organic acid metabolism(parent)
Quick Facts
- SNOMED CT
- 16784003
- UMLS CUI
- C0268641
- Fully Specified Name
- Amino acid transport disorder (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.