cystinuria, nos

Preferred Label : cystinuria, nos;

Details

Origin ID

D6-B8200;

UMLS CUI

C0010691;

Currated CISMeF NLP mapping
- Cystine urine [MedDRA Preferred Term]
- Cystine urine present [MedDRA Preferred Term]
- Cystinosis [ORDO Disease]
- Cystinosis [MedDRA Preferred Term]
- Cystinuria [PASCAL descriptor]
- Cystinuria [ICD-11 Subcategory]
- Cystinuria [NCIt concept]
- Cystinuria [OMIM Phenotype]
- Cystinuria [MedDRA Preferred Term]
- Cystinuria [HPO term]
- Cystinuria [ORDO Disease]
- Cystinuria (disorder) [SNOMED CT concept]
- Cystinuria type A [ORDO Disease]
- 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)]
- Hartnup disease [MedDRA Preferred Term]
- Hartnup disease [PASCAL descriptor]
- Hartnup disorder [OMIM Phenotype]
- cystinosis [MeSH Descriptor]
- cystinosis [Disease (Nov.)]
- cystinuria [Disease (Nov.)]
- cystinuria [CISMeF Querying Strategy]
- cystinuria [DO Concept]
- cystinuria [MeSH Descriptor]
- cystinuria [MeSH concept]
- cystinuria, type A [MeSH concept]
- hartnup disease [MeSH concept]
ICD-10 exact mapping(s)
- Disorders of amino-acid transport [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Cystinuria type B [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Genetic renal tubular disease [ORDO Disease]
- Rare renal tubular disease [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Cystinuria (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cystinuria [OMIM Phenotype]
- Cystinuria [MedDRA Preferred Term]
- Cystinuria [HPO term]
- Cystinuria [NCIt concept]
- Cystinuria (disorder) [SNOMED CT concept]
- cystinuria [CISMeF Querying Strategy]
- cystinuria [MeSH concept]
- cystinuria [DO Concept]
- cystinuria [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

Main resources

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