Congenital immunodeficiency disease	Congenital malformation	Disorder of pigmentation	Disorder of tyrosine metabolism	Immunodeficiency associated with multiple organ system abnormalities
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Hypopigmentation-immunodeficiency disease (disorder)
	Hypopigmentation-immunodeficiency disease
	Partial albinism with immunodeficiency Griscelli syndrome Chediak-Higashi-like syndrome Griscelli syndrome with immunodeficiency
	immunodeficiëntie met hypopigmentatie
	immuundeficiëntie met hypopigmentatie syndroom van Griscelli

Id	37548006
Status	Primitive

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

Associated morphology	Decreased melanin pigmentation
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E70.3
Rule	TRUE
Advice	ALWAYS E70.3
Correlation	SNOMED CT source code to target map code correlation not specified