Rudd Klimek syndrome MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Rudd Klimek syndrome
Unique ID: C535879
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535879
Entry Term(s): Caudal dysgenesis familial type; Familial caudal dysgenesis
Registry Numbers: 0
Heading Mapped to: Cauda Equina / abnormalities; *Ectromelia
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Rudd Klimek syndrome Preferred

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