Autosomal recessive SCID (severe combined immunodeficiency disease)	Severe combined immunodeficiency with low T- and B-cell numbers
\|	\|

Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency (disorder)
	Severe combined immunodeficiency due to LCK deficiency
	Severe combined immunodeficiency due to LCK (lymphocyte-specific protein-tyrosine kinase) deficiency Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency
	A rare combined T- and B-cell immunodeficiency with characteristics of failure to thrive, severe diarrhea, opportunistic infections and abnormal T-cell differentiation and function due to LCK deficiency, leading to an important risk factor for inflammation and autoimmunity.
	ernstige gecombineerde immunodeficiëntie door deficiëntie van 'lymphocyte-specific protein-tyrosine kinase'
	ernstige gecombineerde immunodeficiëntie door LCK-deficiëntie

Id	783617001
Status	Primitive

Finding site	Structure of immune system
Occurrence	Congenital
Pathological process	Abnormal immune process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	D81.1
Rule	TRUE
Advice	ALWAYS D81.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified