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Wiskott-Aldrich syndrome

^ http://purl.obolibrary.org/obo/DOID_9169


A X-linked recessive disease that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia). [ url:https://ghr.nlm.nih.gov/condition/wiskott-aldrich-syndrome ]

Synonyms: Wiskott syndrome

Term info

database cross reference
  • NCI:C3448
  • MESH:D014923
  • OMIM:301000
  • UMLS_CUI:C0043194
  • ICD9CM:279.12
  • ICD10CM:D82.0
  • CSP2005:1849-0285
  • SNOMEDCT_US_2018_03_01:36070007
Subsets

NCIthesaurus

comment

OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:9169

Term relations