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Rh-Null Disease, Amorph Type MeSH Supplementary Concept Data 2025


MeSH Supplementary
Rh-Null Disease, Amorph Type
Unique ID
C566210
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566210
Registry Numbers
0
Heading Mapped to
*Anemia, Hemolytic, Congenital
Frequency
1
Date of Entry
2012/11/05
Revision Date
1955/01/01
Rh-Null Disease, Amorph Type Preferred
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