Laterality Defects, Autosomal Dominant MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Laterality Defects, Autosomal Dominant
Unique ID: C563391
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563391
Registry Number: 0
Heading Mapped to: *Heterotaxy Syndrome
Frequency: 4
Date of Entry: 2012/11/05

Laterality Defects, Autosomal Dominant Preferred

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