Steinfeld Syndrome MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Steinfeld Syndrome
Unique ID: C566655
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566655
Registry Numbers: 0
Heading Mapped to: *Heart Defects, Congenital; *Holoprosencephaly; *Limb Deformities, Congenital
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2012/11/16

Steinfeld Syndrome Preferred

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