Heterotaxy, Visceral, 3, Autosomal MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Heterotaxy, Visceral, 3, Autosomal
Unique ID: C565237
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565237
Registry Numbers: 0
Heading Mapped to: *Heterotaxy Syndrome
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Heterotaxy, Visceral, 3, Autosomal Preferred

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