amino acid transport disorders, inborn

Preferred Label : amino acid transport disorders, inborn;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0328095;

UMLS CUI

C0751746;

Currated CISMeF NLP mapping
- Disorder of amino acid absorption and transport [ORDO Disease]
- Disorders of amino-acid transport [ICD-10 Sub-category]
- Disorders of amino-acid transport [ICD-10 Sub-category (who)]
- amino acid transport disorder, nos [SNOMED Notion]
Related record
- amino acid transport disorders, inborn [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Cystinuria [ICD-11 Subcategory]