MeSH Browser

MeSH Supplementary: Schwartz Cohen-Addad Lambert syndrome
Unique ID: C535835
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535835
Entry Term(s): Congenital melanocytosis with myelomeningocele and hydrocephalus
Registry Numbers: 0
Heading Mapped to: *Hydrocephalus; Melanosis / congenital; *Meningomyelocele
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Schwartz Cohen-Addad Lambert syndrome MeSH Supplementary Concept Data 2025