Congenital immunodeficiency disease	Congenital malformation	Disorder of pigmentation	Disorder of tyrosine metabolism	Immunodeficiency associated with multiple organ system abnormalities
\|	\|	\|	\|	\|

Hypopigmentation-immunodeficiency disease (disorder)
	Hypopigmentation-immunodeficiency disease
	Partial albinism with immunodeficiency Griscelli syndrome Chediak-Higashi-like syndrome Griscelli syndrome with immunodeficiency

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

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E70.3
Term	Albinisme

SNOMED CT to ICD-10 extended map

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

|

Griscelli syndrome type 1

Griscelli syndrome type 3