Terms & Properties

Preferred Name:  LCK-Associated Immunodeficiency

Definition:  An extremely rare autosomal recessive condition caused by mutation(s) in the LCK gene, encoding tyrosine-protein kinase Lck. It is characterized by T-cell dysfunction.

Label:  LCK-Associated Immunodeficiency

NCI Thesaurus Code:  C176808 (Search for linked caDSR metadata)   (search value sets)

NCI Metathesaurus Link:  C4016253  (see NCI Metathesaurus info)

Synonyms & Abbreviations: (see Synonym Details)

IMD22

Immunodeficiency 22

LCK Deficiency

LCK Deficiency (T Lymphocyte-specific protein TK)

LCK-Associated Immunodeficiency

External Source Codes: 

UMLS CUI

C4016253

Other Properties:

Name	Value (qualifiers indented underneath)
code	C176808
Semantic_Type	Disease or Syndrome

Additional Concept Data: 

Defined Fully by Roles: No

URL:https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&ns=ncit&code=C176808