MeSH Browser

MeSH Supplementary: Hermansky Pudlak syndrome 2
Unique ID: C537709
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537709
Entry Term(s): Hermansky-Pudlak syndrome 2; Platelet defects and oculocutaneous albinism
Heading Mapped to: *Hermanski-Pudlak Syndrome
Frequency: 19
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Hermansky Pudlak syndrome 2 MeSH Supplementary Concept Data 2024