lymphoproliferative syndrome, X-Linked, 2

Preferred Label : lymphoproliferative syndrome, X-Linked, 2;

MeSH note : mutation in XIAP;

MeSH synonym : XIAP deficiency;

Origin ID

C564469;

UMLS CUI

C1845076;

Automatic exact mappings (from CISMeF team)
- X-linked lymphoproliferative disease due to XIAP deficiency [ORDO Disease]
Currated CISMeF NLP mapping
- Lymphoproliferative syndrome, X-linked, 2 [OMIM Phenotype]
- X-linked Lymphoproliferative Syndrome 2 [NCIt concept]
- X-linked lymphoproliferative disease due to XIAP deficiency (disorder) [SNOMED CT concept]
- X-linked lymphoproliferative syndrome 2 [DO Concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- lymphoproliferative disorders [MeSH Descriptor]
Record concept(s)
- lymphoproliferative syndrome, X-Linked, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphoproliferative syndrome, X-linked, 2 [OMIM Phenotype]
- X-linked Lymphoproliferative Syndrome 2 [NCIt concept]
- X-linked lymphoproliferative disease due to XIAP deficiency (disorder) [SNOMED CT concept]
- X-linked lymphoproliferative syndrome 2 [DO Concept]