hemophagocytic lymphohistiocytosis, familial, 2

Preferred Label : hemophagocytic lymphohistiocytosis, familial, 2;

Origin ID

C537250;

UMLS CUI

C1863727;

Currated CISMeF NLP mapping
- Hemophagocytic lymphohistiocytosis, familial, 2 [OMIM Phenotype]
- familial hemophagocytic lymphohistiocytosis 2 [DO Concept]
MeSH term(s) associated for indexing
- lymphohistiocytosis, hemophagocytic [MeSH Descriptor]
Record concept(s)
- Hemophagocytic lymphohistiocytosis, familial, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hemophagocytic lymphohistiocytosis, familial, 2 [OMIM Phenotype]
- familial hemophagocytic lymphohistiocytosis 2 [DO Concept]