exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis

Preferred Label : exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis;

Origin ID

C567195;

UMLS CUI

C2675184;

CISMeF manual mappings
- Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- anemia, dyserythropoietic, congenital [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- exocrine pancreatic insufficiency [MeSH Descriptor]
- hyperostosis [MeSH Descriptor]
Record concept(s)
- exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis [OMIM Phenotype]
- Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) [SNOMED CT concept]
- Pancreatic insufficiency-anemia-hyperostosis syndrome [ORDO Disease]