MeSH Browser

MeSH Supplementary: Verloes Van Maldergem Marneffe syndrome
Unique ID: C536540
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536540
Entry Term(s): Dominantly inherited bone dysplasia with severe eye involvement; Microspherophakia-metaphyseal dysplasia
Registry Number: 0
Heading Mapped to: Lens, Crystalline / *abnormalities; *Osteochondrodysplasias
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Verloes Van Maldergem Marneffe syndrome MeSH Supplementary Concept Data 2023