MeSH Browser

MeSH Supplementary: Mesomelic dwarfism Reinhardt Pfeiffer type
Unique ID: C537349
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537349
Entry Term(s): Hypoplasia of Ulna and Fibula; Mesomelic dwarfism of hypoplastic ulna and fibula type; Reinhardt Pfeiffer syndrome; Reinhardt-Pfeiffer mesomelic dysplasia; Reinhardt-Pfeiffer mesomelic skeletal dysplasia; Ulna And Fibula, Hypoplasia Of
Registry Numbers: 0
Heading Mapped to: *Dwarfism; Fibula / abnormalities; *Osteochondrodysplasias; Ulna / abnormalities
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Mesomelic dwarfism Reinhardt Pfeiffer type MeSH Supplementary Concept Data 2025