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Heterotaxy, Visceral, 3, Autosomal MeSH Supplementary Concept Data 2023


MeSH Supplementary
Heterotaxy, Visceral, 3, Autosomal
Unique ID
C565237
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565237
Registry Number
0
Heading Mapped to
*Heterotaxy Syndrome
Frequency
0
Date of Entry
2012/11/05
Heterotaxy, Visceral, 3, Autosomal Preferred
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