MeSH Browser

MeSH Supplementary: Klippel Feil syndrome recessive type
Unique ID: C536888
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536888
Entry Term(s): Cervical vertebral fusion, autosomal recessive; Kfs, Autosomal Recessive; Klippel-Feil Syndrome, Autosomal Recessive
Registry Number: 0
Heading Mapped to: *Klippel-Feil Syndrome
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Klippel Feil syndrome recessive type MeSH Supplementary Concept Data 2023