MeSH Browser

MeSH Supplementary: Schaefer Stein Oshman syndrome
Unique ID: C536627
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536627
Entry Term(s): Craniodiaphyseal dysplasia, dominant; Dominantly inherited craniodiaphyseal dysplasia
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Osteochondrodysplasias; *Craniofacial Abnormalities
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Schaefer Stein Oshman syndrome MeSH Supplementary Concept Data 2024