Alpha-1-antitrypsin deficiency

ICD-11 code : 5C5A;

Preferred Label : Alpha-1-antitrypsin deficiency;

ICD-11 definition : Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterized by low serum levels of AAT, the main protease inhibitor (PI) in human serum.;

ICD-11 synonym : AATD - [Alpha-1-antitrypsin] deficiency; AATD deficiency;

Détails

Origin ID

824872160;

Currated CISMeF NLP mapping
- Alpha 1 antitrypsine deficiency [PASCAL descriptor]
- Alpha-1 Antitrypsin Deficiency [NCIt concept]
- Alpha-1-antitrypsin deficiency [ICD-9 code]
- Alpha-1-antitrypsin deficiency [ORDO Disease]
- Alpha-1-antitrypsin deficiency [OMIM Phenotype]
- Alpha-1-antitrypsin deficiency (disorder) [SNOMED CT concept]
- Disorders of plasma-protein metabolism, not elsewhere classified [ICD-10 Sub-category]
- alpha 1 antitrypsin deficiency [Disease (Nov.)]
- alpha 1-Antitrypsin deficiency [MeSH concept]
- alpha 1-antitrypsin deficiency [MeSH Descriptor]
- alpha 1-antitrypsin deficiency [DO Concept]
- alpha-1 anti-trypsin deficiency [MedDRA Preferred Term]
- alpha-1 antitrypsin deficiency [MedlinePlus Topic]
- alpha-1-antitrypsin deficiency [SNOMED Notion]
ICD-10 Mapping
- Disorders of plasma-protein metabolism, not elsewhere classified [ICD-10 Sub-category]
Validated automatic mappings to NTBT
- Disorders of plasma-protein metabolism, not elsewhere classified [ICD-10 Sub-category]

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

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