Hermansky pudlak syndrome
A group of autosomal recessive inherited disorders characterized by albinism, bleeding tendency, and lung disorders such as pulmonary fibrosis.
Syndrome characterized by the triad of oculocutaneous albinism albinism, oculocutaneous); platelet storage pool deficiency; and lysosomal accumulation of ceroid lipofuscin.
E70.331 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM E70.331 became effective on October 1, 2022.
This is the American ICD-10-CM version of E70.331 – other international versions of ICD-10 E70.331 may differ.