Autoimmune Lymphoproliferative Syndrome

Preferred Label : Autoimmune Lymphoproliferative Syndrome;

NCIt synonyms : Canale-Smith Syndrome; ALPS;

NCIt related terms : Autoimmune Lymphoproliferative Syndrome (ALPS);

NCIt definition : An autoimmune hematologic disorder characterized by autoimmune hemolytic anemia, thrombocytopenia, lymphadenopathy, hepatomegaly and splenomegaly. Patients are at an increased risk of developing Hodgkin and non-Hodgkin lymphomas.;

Details

Origin ID

C37864;

UMLS CUI

C1328840;

Currated CISMeF NLP mapping
- Autoimmune lymphoproliferative syndrome [PASCAL descriptor]
- Autoimmune lymphoproliferative syndrome [ICD-11 More detail]
- Autoimmune lymphoproliferative syndrome [ICD-9 code]
- Autoimmune lymphoproliferative syndrome [MedDRA Preferred Term]
- Autoimmune lymphoproliferative syndrome [OMIM Phenotype]
- Autoimmune lymphoproliferative syndrome [ORDO Disease]
- Autoimmune lymphoproliferative syndrome (disorder) [SNOMED CT concept]
- autoimmune lymphoproliferative syndrome [DO Concept]
- autoimmune lymphoproliferative syndrome [Disease (Nov.)]
- autoimmune lymphoproliferative syndrome [MeSH Descriptor]
- autoimmune lymphoproliferative syndrome [MeSH concept]
DO Cross reference
- autoimmune lymphoproliferative syndrome [DO Concept]
Disease may have findings
- Hepatomegaly [NCIt concept]
- Interleukin-10 Overexpression [NCIt concept]
- Lymphadenopathy [NCIt concept]
- Splenomegaly [NCIt concept]
- Thrombocytopenia [NCIt concept]
False automatic mappings
- 1-hydroxy-2-[(6-o-.beta.-d-xylopyranosyl-.beta.-d-glucopyranosyl)oxy]anthraquinone [Substance BNPC]
- Atherosclerosis susceptibility [OMIM Phenotype]
- ruberythric acid [MeSH concept]
- ruberythric acid [MeSH Supplementary Concept]
Has associated anatomic sites
- Immune System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autoimmune lymphoproliferative syndrome [ORDO Disease]
- Autoimmune lymphoproliferative syndrome [MedDRA Preferred Term]
- Autoimmune lymphoproliferative syndrome [OMIM Phenotype]
- Autoimmune lymphoproliferative syndrome [PASCAL descriptor]
- Autoimmune lymphoproliferative syndrome [ICD-9 code]
- Autoimmune lymphoproliferative syndrome [ICD-11 More detail]
- Autoimmune lymphoproliferative syndrome (disorder) [SNOMED CT concept]
- autoimmune lymphoproliferative syndrome [DO Concept]
- autoimmune lymphoproliferative syndrome [Disease (Nov.)]
- autoimmune lymphoproliferative syndrome [MeSH concept]
- autoimmune lymphoproliferative syndrome [MeSH Descriptor]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
disease_has_abnormal_cell
- Reactive Lymphocyte [NCIt concept]
disease_has_associated_disease
- Autoimmune Lymphoproliferative Syndrome-Related Lymphoma [NCIt concept]
disease_has_normal_cell_origin
- Lymphocyte [NCIt concept]
disease_may_have_abnormal_cell
- Atypical Lymphocyte [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
- Autoimmune Disease [NCIt concept]
- Autoimmune Lymphoproliferative Syndrome-Related Lymphoma [NCIt concept]
- Lymphoproliferative Disease Associated with Primary Immune Disorder [NCIt concept]
- Rosai-Dorfman-Destombes Disease [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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