Pancreatic insufficiency, combined exocrine

Preferred Label : Pancreatic insufficiency, combined exocrine;

Obsolete resource : true;

Moved to : 243800;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 260450;

Details

Origin ID

260450;

UMLS CUI

C1850081;

Currated CISMeF NLP mapping
- pancreatic insufficiency, combined exocrine [MeSH concept]
- pancreatic insufficiency, combined exocrine [MeSH Supplementary Concept]
HPO term(s)
- Anal atresia [HPO term]
- Anasarca [HPO term]
- Autosomal recessive inheritance [HPO term]
- Congestive heart failure [HPO term]
- Exocrine pancreatic insufficiency [HPO term]
- Hypoproteinemia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- pancreatic insufficiency, combined exocrine [MeSH Supplementary Concept]
- pancreatic insufficiency, combined exocrine [MeSH concept]

Keyword's position in hierarchy(ies) :

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