Autoimmune Lymphoproliferative Syndrome with Germline FADD Mutation

Preferred Label : Autoimmune Lymphoproliferative Syndrome with Germline FADD Mutation;

NCIt synonyms : ALPS with Germline FADD Mutation;

NCIt definition : Autoimmune lymphoproliferative syndrome characterized by the presence of germline FADD mutation.;

NCI Metathesaurus CUI : CL1915438;

Details

Origin ID

C201057;

UMLS CUI

C5856605;

Disease may have findings
- Hepatomegaly [NCIt concept]
- Interleukin-10 Overexpression [NCIt concept]
- Lymphadenopathy [NCIt concept]
- Splenomegaly [NCIt concept]
- Thrombocytopenia [NCIt concept]
Has associated anatomic sites
- Immune System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
disease_excludes_molecular_abnormality
- FAS Gene Mutation [NCIt concept]
disease_has_abnormal_cell
- Reactive Lymphocyte [NCIt concept]
disease_has_molecular_abnormality
- Germline FADD Gene Mutation [NCIt concept]
- Germline Variation [NCIt concept]
disease_has_normal_cell_origin
- Lymphocyte [NCIt concept]
disease_mapped_to_gene
- FADD Gene [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]
pathogenesis_of_disease_involves_gene
- FADD Gene [NCIt concept]
- FADD wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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