MeSH Browser

MeSH Supplementary: Oculocerebral hypopigmentation syndrome type Preus
Unique ID: C537866
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537866
Entry Term(s): Cross syndrome; Kramer Syndrome; Oculocerebral Hypopigmentation Syndrome of Preus; Oculocerebral syndrome with hypopigmentation
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Pigmentation Disorders; *Craniofacial Abnormalities
Frequency: 11
Date of Entry: 2010/08/25
Revision Date: 2017/09/22

Oculocerebral hypopigmentation syndrome type Preus MeSH Supplementary Concept Data 2025