Immunodeficiency following hereditary defective response to Epstein-Barr virus

Preferred Label : Immunodeficiency following hereditary defective response to Epstein-Barr virus;

Inclusion CIM-10 : X-linked lymphoproliferative disease;

Diag associé à un acte (%) : 58.6;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D823;

UMLS CUI

C0451697;

Automatic exact mappings (from CISMeF team)
- Lymphoproliferative syndrome, X-linked, 1 [OMIM Phenotype]
- lymphoproliferative disorders [MeSH Descriptor]
Currated CISMeF NLP mapping
- Duncan disease [PASCAL descriptor]
- Immunodeficiency following hereditary defective response to Epstein-Barr virus [ICD-10 Sub-category (who)]
- Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder) [SNOMED CT concept]
- X-Linked lymphoproliferative disorder [MeSH concept]
- X-linked lymphoproliferative disease [ICD-11 More detail]
- X-linked lymphoproliferative disorder [Disease (Nov.)]
- X-linked lymphoproliferative syndrome [MedDRA Preferred Term]
- X-linked lymphoproliferative syndrome (disorder) [SNOMED CT concept]
- x-linked lymphoproliferative syndrome [SNOMED Notion]
DO Cross reference
- X-linked lymphoproliferative syndrome 1 [DO Concept]
- X-linked lymphoproliferative syndrome 2 [DO Concept]
Orphanet concepts
- Combined immunodeficiency due to CARMIL2 deficiency [ORDO Disease]
- Combined immunodeficiency due to CD70 deficiency [ORDO Disease]
- Combined immunodeficiency due to ITK deficiency [ORDO Disease]
- X-linked lymphoproliferative disease [ORDO Disease]
- X-linked lymphoproliferative disease due to SH2D1A deficiency [ORDO Disease]
- X-linked lymphoproliferative disease due to XIAP deficiency [ORDO Disease]
See also inter- (CISMeF)
- X-linked lymphoproliferative disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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