MeSH Browser

MeSH Supplementary: Griscelli syndrome type 1
Unique ID: C537301
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537301
Entry Term(s): Griscelli Syndrome, Type 1; Griscelli syndrome with neurologic impairment; Griscelli syndrome, cutaneous and neurologic type; Partial albinism and primary neurologic disease without hemophagocytic syndrome
Heading Mapped to: *Hearing Loss, Sensorineural; *Pigmentation Disorders; *Piebaldism
Frequency: 14
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Griscelli syndrome type 1 MeSH Supplementary Concept Data 2024