Autosomal recessive hereditary disorder	Combined immunodeficiency disease
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Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder)
	Combined immunodeficiency due to MALT1 deficiency
	Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency
	A rare genetic form of primary immunodeficiency with characteristics of growth retardation, early recurrent pulmonary infections leading to bronchiectasis, inflammatory gastrointestinal disease, and other symptoms, such as rash, dermatitis, skin infections. Caused by homozygous mutation in the MALT1 gene on chromosome 18q21.
	gecombineerde immuundeficiëntie door MALT1-deficiëntie
	gecombineerde immunodeficiëntie door deficiëntie van 'mucosa-associated lymphoid tissue lymphoma translocation gene 1'

Id	773488000
Status	Primitive

Pathological process

Abnormal immune process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	D81.8
Rule	TRUE
Advice	ALWAYS D81.8
Correlation	SNOMED CT source code to target map code correlation not specified