Emphysema, hereditary pulmonary

Preferred Label : Emphysema, hereditary pulmonary;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Familial factors over and above alpha1-antitrypsin;

Prefixed ID : 130700;

Détails

Origin ID

130700;

UMLS CUI

C1851718;

Automatic exact mappings (from CISMeF team)
- alpha-1-Antitrypsin deficiency, autosomal recessive [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- emphysema, hereditary pulmonary [MeSH concept]
- emphysema, hereditary pulmonary [MeSH Supplementary Concept]
- hereditary emphysema [Disease (Nov.)]
DO Cross reference
- pulmonary emphysema [DO Concept]
HPO term(s)
- Chronic bronchitis [HPO term]
- Chronic pulmonary obstruction [HPO term]
- Emphysema [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- emphysema, hereditary pulmonary [MeSH Supplementary Concept]
- emphysema, hereditary pulmonary [MeSH concept]
- hereditary emphysema [Disease (Nov.)]

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

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