MeSH Browser

MeSH Supplementary: Griscelli syndrome type 3
Unique ID: C537303
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537303
Entry Term(s): Griscelli Syndrome, Type 3; Hypomelanosis with no immunologic or neurologic manifestations
Registry Number: 0
Heading Mapped to: *Pigmentation Disorders; *Piebaldism
Frequency: 14
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Griscelli syndrome type 3 MeSH Supplementary Concept Data 2024