Aplasia cutis congenita intestinal lymphangiectasia

Preferred Label : Aplasia cutis congenita intestinal lymphangiectasia;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0532249;

UMLS CUI

C1859753;

CISMeF manual mappings
- Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Aplasia cutis congenita - intestinal lymphangiectasia [ICD-11 More detail]
- Aplasia cutis congenita with intestinal lymphangiectasia [OMIM Phenotype]
- Aplasia cutis congenita-intestinal lymphangiectasia syndrome [ORDO Disease]
Related record
- aplasia cutis congenita intestinal lymphangiectasia [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aplasia cutis congenita with intestinal lymphangiectasia [OMIM Phenotype]
- Aplasia cutis congenita-intestinal lymphangiectasia syndrome [ORDO Disease]