MeSH Browser

MeSH Supplementary: Klippel Feil syndrome dominant type
Unique ID: C536887
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536887
Entry Term(s): Cervical vertebral fusion, autosomal dominant; Klippel-Feil syndrome, autosomal dominant
Registry Numbers: 0
Heading Mapped to: *Klippel-Feil Syndrome
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Klippel Feil syndrome dominant type MeSH Supplementary Concept Data 2025