congenital pancreatic trypsin deficiency

Preferred Label : congenital pancreatic trypsin deficiency;

Origin ID

D5-90520;

UMLS CUI

C0267961;

Currated CISMeF NLP mapping
- Congenital pancreatic trypsin deficiency (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other specified metabolic disorders [ICD-10 Sub-category (who)]
Metaterm(s)
- gastroenterology [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- pancreas, nos [SNOMED Notion]
- trypsin [SNOMED Notion]
SNOMED CT concept
- Congenital pancreatic trypsin deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital pancreatic trypsin deficiency (disorder) [SNOMED CT concept]