Dense body defect	Tyrosinase-positive oculocutaneous albinism
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Hermansky-Pudlak syndrome (disorder)
	Hermansky-Pudlak syndrome
	Albinism with hemorrhagic diathesis Hermansky Pudlak syndrome Alpha storage pool disease
	Hermansky-Pudlak-syndroom
	syndroom van Hermansky-Pudlak HPS

Id	9311003
Status	Primitive

Associated morphology	Decreased melanin pigmentation
Finding site	Skin structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Decreased melanin pigmentation
Finding site	Eye structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Abnormal
Interprets	Hemostatic function

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