syndromic oculocutaneous albinism disorder of lysosomal-related organelles Hermansky-Pudlak syndrome https://www.malacards.org/card/hermansky_pudlak_syndrome Hepatopulmonary Syndrome ICD9:270.2 MEDGEN:36313 GARD:0006643 Hermansky Pudlak syndrome HPS (Hermansky Pudlak syndrome) Hermansky-Pudlak syndrome (HSP) is a multi-system disorder characterized by oculocutaneous albinism, bleeding diathesis and, in some cases, neutropenia, pulmonary fibrosis, or granulomatous colitis. HPS comprises eight known disorders (HPS-1 to HPS-8), the majority of which present with the same clinical phenotype to varying degrees of severity. NCIT:C37261 NORD:1918 MESH:D022861 Orphanet:79430 UMLS:C0079504 SCTID:9311003 OMIMPS:203300 ICD10CM:E70.331 MONDO:0019312 NANDO:1200638 icd11.foundation:2089801290 HPS MedDRA:10071775 DOID:3753 inherited blood coagulation disorder