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Steinfeld Syndrome MeSH Supplementary Concept Data 2023


MeSH Supplementary
Steinfeld Syndrome
Unique ID
C566655
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566655
Registry Number
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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