Disorders of tyrosine metabolism

Preferred Label : Disorders of tyrosine metabolism;

ICD-10 exclusion note : transitory tyrosinemia of newborn (P74.5);

Diag associé à un acte (%) : 82.2;

Source : OMS;

Date de début : 01/01/1997;

Détails

Origin ID

E702;

UMLS CUI

C0268482;

Automatic exact mappings (from CISMeF team)
- Ochronosis [NCIt concept]
- Ochronosis, hereditary [MeSH concept]
- alkaptonuria [MeSH concept]
- ochronosis [MeSH Descriptor]
Currated CISMeF NLP mapping
- Abnormal circulating tyrosine concentration [HPO term]
- Disorder of tyrosine metabolism [ORDO Disease]
- Disorder of tyrosine metabolism (disorder) [SNOMED CT concept]
- Disorders of tyrosine metabolism [ICD-11 Subcategory]
- disorders of tyrosine metabolism [Error of metabolism category]
- disorders of tyrosine metabolism [Artificial nutrition thesaurus concept]
- disturbance of tyrosine metabolism, nos [SNOMED Notion]
Excluded by
- Other articular cartilage disorders [ICD-10 Sub-category]
Orphanet concepts
- Alkaptonuria [ORDO Disease]
- Disorder of tyrosine metabolism [ORDO Disease]
- Hawkinsinuria [ORDO Disease]
- Tyrosinemia type 1 [ORDO Disease]
- Tyrosinemia type 2 [ORDO Disease]
- Tyrosinemia type 3 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder of tyrosine metabolism [ORDO Disease]
- Disorder of tyrosine metabolism (disorder) [SNOMED CT concept]
- Disorders of tyrosine metabolism [ICD-11 Subcategory]
- disturbance of tyrosine metabolism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Alkaptonuria [ICD-11 Sub-sub category]
- Systemic disorders of connective tissue in other diseases classified elsewhere [ICD-10 Sub-category (who)]
- Tyrosinaemia type 1 [ICD-11 Sub-sub category]
- Tyrosinaemia type 2 [ICD-11 Sub-sub category]
- Tyrosinemia [NCIt concept]
- alkaptonuria [MeSH Descriptor]
- ochronosis [MeSH concept]
- tyrosinosis [MeSH concept]
- tyrosinosis [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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