metabolic disease, nos - CISMeF

CISMeF

chu

Metabolic disease, nosSNOMED Notion

Preferred Label : metabolic disease, nos;

Details

Origin ID

D6-00000;

UMLS CUI

C0025517;

Currated CISMeF NLP mapping
- Congenital Metabolic Disorder [NCIt concept]
- Inborn error of metabolism [MedDRA Preferred Term]
- Inborn error of metabolism (disorder) [SNOMED CT concept]
- Inborn error of metabolism NOS [MedDRA LLT]
- Inborn errors of metabolism [MedDRA High Level Group Term]
- Metabolic Disorder [NCIt concept]
- Metabolic disease [EDAM topic]
- Metabolic disease (disorder) [SNOMED CT concept]
- Metabolic diseases [PASCAL descriptor]
- Metabolic disorder [MedDRA Preferred Term]
- Metabolic disorder [PASCAL descriptor]
- Metabolic disorder NOS [MedDRA LLT]
- Metabolic disorder, unspecified [ICD-10 Sub-category]
- Metabolic disorder, unspecified [ICD-10 Sub-category (who)]
- Metabolic disorders [ICD-10 Block (who)]
- Metabolic disorders [Bloc CIM-11]
- Metabolic disorders [HPMULTI term]
- Other metabolic disorders [Bloc CIM-11]
- Rare inborn errors of metabolism [ORDO Disease]
- Unspecified disorder of metabolism [ICD-9 code]
- disease of metabolism [DO Concept]
- inherited metabolic disorder [DO Concept]
- metabolic disease [Radlex concept]
- metabolic disease [COVID-19 Thesaurus concept]
- metabolic diseases [MeSH Descriptor]
- metabolic diseases [MeSH concept]
- metabolic disorder [Disease (Nov.)]
- metabolic disorder [Artificial nutrition thesaurus concept]
- metabolic disorders [MedlinePlus Topic]
- metabolism, inborn errors [MeSH Descriptor]
- metabolism, inborn errors [MeSH concept]
Décrit
- arthropathy associated with an endocrine or metabolic disorder [SNOMED Notion]
- dilated cardiomyopathy secondary to metabolic disorder [SNOMED Notion]
- metabolic bone disease, nos [SNOMED Notion]
ICD-10 exact mapping(s)
- Metabolic disorder, unspecified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Autosomal dominant myoglobinuria [ORDO Disease]
- Blue diaper syndrome [ORDO Disease]
- Classic glucose transporter type 1 deficiency syndrome [ORDO Disease]
- Congenital brain dysgenesis due to glutamine synthetase deficiency [ORDO Disease]
- Disorder of energy metabolism [ORDO Disease]
- Genetic recurrent myoglobinuria [ORDO Disease]
- Hereditary hypercarotenemia and vitamin A deficiency [ORDO Disease]
- Hyperdibasic aminoaciduria type 1 [ORDO Disease]
- McLeod neuroacanthocytosis syndrome [ORDO Disease]
- Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency [ORDO Disease]
- Transient tyrosinemia of the newborn [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Metabolic diseases with epilepsy [ORDO Disease]
- Rare genetic disease [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- disease, nos [SNOMED Notion]
- general metabolic function, nos [SNOMED Notion]
SNOMED CT concept
- Metabolic disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Generalized metabolic disorder (disorder) [SNOMED CT concept]
- Metabolic Disorder [NCIt concept]
- Metabolic disease (disorder) [SNOMED CT concept]
- Metabolic diseases [PASCAL descriptor]
- Metabolic disorder [MedDRA Preferred Term]
- Metabolic disorder [PASCAL descriptor]
- Metabolic disorder NOS [MedDRA LLT]
- Metabolic disorder, unspecified [ICD-10 Sub-category]
- Metabolic disorders [ICD-10 Block (who)]
- Metabolic disorders [Bloc CIM-11]
- Other metabolic disorders [Bloc CIM-11]
- Rare inborn errors of metabolism [ORDO Disease]
- Unspecified disorder of metabolism [MedDRA LLT]
- Unspecified disorder of metabolism [ICD-9 code]
- disease of metabolism [DO Concept]
- metabolic disease [Radlex concept]
- metabolic diseases [MeSH Descriptor]
- metabolic diseases [MeSH concept]
- metabolic disorder [Disease (Nov.)]
- metabolic disorders [MedlinePlus Topic]

Keyword's position in hierarchy(ies) :

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14/05/2024

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