Cystinuria - CISMeF

ICD-11 code : 5C60.2;

Preferred Label : Cystinuria;

ICD-11 definition : Cystinuria is a renal tubular aminoacid transport disorder characterized by recurrent formation of kidneys cystine stones.;

ICD-11 synonym : Cystinuria - lysinuria;

ICD-11 inclusion : CSNU - [cystinuria]; cystine disease;

Details

Origin ID

1237620397;

Currated CISMeF NLP mapping
- Amino acid transport disorder (disorder) [SNOMED CT concept]
- Cystine urine present [MedDRA Preferred Term]
- Cystinosis [ORDO Disease]
- Cystinosis [MedDRA Preferred Term]
- Cystinuria [ORDO Disease]
- Cystinuria [MedDRA Preferred Term]
- Cystinuria [PASCAL descriptor]
- Cystinuria [OMIM Phenotype]
- Cystinuria [NCIt concept]
- Cystinuria [HPO term]
- Cystinuria (disorder) [SNOMED CT concept]
- Disorder of amino acid absorption and transport [ORDO Disease]
- Disorders of amino-acid transport [ICD-10 Sub-category]
- Hartnup disease [MedDRA Preferred Term]
- Hartnup disease [PASCAL descriptor]
- Hartnup disorder [OMIM Phenotype]
- cystinosis [MeSH Descriptor]
- cystinosis [Disease (Nov.)]
- cystinuria [CISMeF Querying Strategy]
- cystinuria [MeSH concept]
- cystinuria [DO Concept]
- cystinuria [MeSH Descriptor]
- cystinuria [Disease (Nov.)]
- cystinuria, nos [SNOMED Notion]
- cystinuria, type A [MeSH concept]
- hartnup disease [MeSH concept]
False automatic mappings
- Fanconi syndrome [Disease (Nov.)]
ICD-10 Mapping
- Disorders of amino-acid transport [ICD-10 Sub-category]
See also inter- (CISMeF)
- Cystine urine [MedDRA Preferred Term]
- Cystinosis [PASCAL descriptor]
- Cystinosis [NCIt concept]
- Cystinosis (disorder) [SNOMED CT concept]
- Cystinosis, nephropathic [OMIM Phenotype]
- Hartnup Disease [NCIt concept]
- Hartnup disease [ORDO Disease]
- Hartnup disease [DO Concept]
- Neutral 1 amino acid transport defect (disorder) [SNOMED CT concept]
- cystinosis [DO Concept]
- cystinosis [MeSH concept]
- cystinosis, nos [SNOMED Notion]
- hartnup disease [MeSH Descriptor]
- neutral 1 amino acid transport defect [SNOMED Notion]
Validated automatic mappings to BTNT
- Cystinuria type A [ORDO Disease]
- Cystinuria type B [ORDO Disease]
- cystinuria, type A [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Amino acid transport disorder (disorder) [SNOMED CT concept]
- Disorders of amino-acid transport [ICD-10 Sub-category (who)]
- amino acid transport disorder, nos [SNOMED Notion]
- amino acid transport disorders, inborn [MeSH concept]
- amino acid transport disorders, inborn [MeSH Descriptor]

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