Wiskott-Aldrich Syndrome

Preferred Label : Wiskott-Aldrich Syndrome;

NCIt synonyms : Wiskott Aldrich Syndrome;

NCIt related terms : Aldrich syndrome;

NCIt definition : A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenia, and recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IgM levels are low and IgA and IgE levels are elevated. Lymphoreticular malignancies are common.;

Alternative definition : NICHD: A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenia, and recurrent pyogenic infection. Typically, IgM levels are low and IgA and IgE levels are elevated. Lymphoreticular malignancies are common.; NCI-GLOSS: An inherited immune disorder that occurs in young boys. It causes eczema (a type of skin inflammation), a decrease in the number of platelets (blood cells that help prevent bleeding), and frequent bacterial infections. People with Wiskott-Aldrich syndrome are at increased risk of developing leukemia and lymphoma.;

Codes from synonyms : CDR0000562657; CDR0000539110;

Details

Origin ID

C3448;

UMLS CUI

C0043194;

Currated CISMeF NLP mapping
- Aldrich syndrome [MedDRA LLT]
- Wiskott Aldrich syndrome [Disease (Nov.)]
- Wiskott-Aldrich syndrome [PASCAL descriptor]
- Wiskott-Aldrich syndrome [ICD-10 Sub-category]
- Wiskott-Aldrich syndrome [DO Concept]
- Wiskott-Aldrich syndrome [ICD-11 More detail]
- Wiskott-Aldrich syndrome [ICD-10 Sub-category (who)]
- Wiskott-Aldrich syndrome [MedDRA Preferred Term]
- Wiskott-Aldrich syndrome [MeSH concept]
- Wiskott-Aldrich syndrome [ORDO Disease]
- Wiskott-Aldrich syndrome (disorder) [SNOMED CT concept]
- Wiskott-aldrich syndrome [ICD-9 code]
- Wiskott-aldrich syndrome [OMIM Phenotype]
- Wiskott-aldrich syndrome [OMIM Phenotype]
- wiskott-aldrich syndrome [MeSH Descriptor]
- wiskott-aldrich syndrome [SNOMED Notion]
DO Cross reference
- Wiskott-Aldrich syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aldrich syndrome [MedDRA LLT]
- Wiskott Aldrich syndrome [Disease (Nov.)]
- Wiskott-Aldrich syndrome [ORDO Disease]
- Wiskott-Aldrich syndrome [ICD-10 Sub-category]
- Wiskott-Aldrich syndrome [PASCAL descriptor]
- Wiskott-Aldrich syndrome [DO Concept]
- Wiskott-Aldrich syndrome [ICD-11 More detail]
- Wiskott-Aldrich syndrome [ICD-10 Sub-category (who)]
- Wiskott-Aldrich syndrome [MedDRA Preferred Term]
- Wiskott-Aldrich syndrome [MeSH concept]
- Wiskott-Aldrich syndrome (disorder) [SNOMED CT concept]
- Wiskott-aldrich syndrome [OMIM Phenotype]
- Wiskott-aldrich syndrome [OMIM Phenotype]
- Wiskott-aldrich syndrome [ICD-9 code]
- wiskott-aldrich syndrome [SNOMED Notion]
- wiskott-aldrich syndrome [MeSH Descriptor]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_has_associated_gene
- WAS Gene [NCIt concept]
- WAS wt Allele [NCIt concept]
disease_has_finding
- Hereditary Lesion [NCIt concept]
disease_has_molecular_abnormality
- WAS Gene Mutation [NCIt concept]
disease_may_have_associated_disease
- Lymphoproliferative Disease Associated with Primary Immune Disorder [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients