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Properdin Deficiency, Type III
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Properdin Deficiency, Type III
Unique ID
C564076
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564076
Registry Number
0
Previous Indexing
IMMUNOLOGIC DEFICIENCY SYNDROMES (2014-2019)
Heading Mapped to
*Hereditary Complement Deficiency Diseases
Properdin
/
*deficiency
*Genetic Diseases, X-Linked
Frequency
0
Date of Entry
2012/11/05
Revision Date
2019/06/17
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Properdin Deficiency, Type III
Preferred
Concept UI
M0564376
Registry Number
0
Terms
Properdin Deficiency, Type III
Preferred Term
Term UI
T829159
Date
09/06/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
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