Syndrome

Hermanski-Pudlak Syndrome

AMW:DIS:110044

Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin.

Pathology clinical

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Hermanski-Pudlak Syndrome has parent Albinism, Oculocutaneous

Hermanski-Pudlak Syndrome has parent Blood Coagulation Disorders, Inherited

Hermanski-Pudlak Syndrome has parent Platelet Storage Pool Deficiency

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