MeSH Browser

MeSH Supplementary: Orofaciodigital Syndrome X
Unique ID: C563491
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563491
Entry Term(s): Oral-Facial-Digital Syndrome with Fibular Aplasia; Oral-Facial-Digital Syndrome, Type X; Orofaciodigital Syndrome with Fibular Aplasia
Registry Numbers: 0
Heading Mapped to: Fibula / abnormalities; *Orofaciodigital Syndromes; Radius / abnormalities
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Orofaciodigital Syndrome X MeSH Supplementary Concept Data 2025