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Properdin Deficiency, Type III MeSH Supplementary Concept Data 2025


MeSH Supplementary
Properdin Deficiency, Type III
Unique ID
C564076
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564076
Registry Numbers
0
Previous Indexing
IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to
Properdin / deficiency
*Genetic Diseases, X-Linked
*Hereditary Complement Deficiency Diseases
Frequency
0
Date of Entry
2012/11/05
Revision Date
2019/06/17
Properdin Deficiency, Type III Preferred
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