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Reticuloendotheliosis, X-linked MeSH Supplementary Concept Data 2025


MeSH Supplementary
Reticuloendotheliosis, X-linked
Unique ID
C538362
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538362
Entry Term(s)
Reticuloendotheliosis
Registry Numbers
0
Heading Mapped to
*Severe Combined Immunodeficiency
*Genetic Diseases, X-Linked
Frequency
873
Note
An X-linked disease where cells of the RETICULOENDOTHELIAL SYSTEM exhibit abnormal growth and proliferation. Onset occurs in infancy and is characterized by fever, JAUNDICE; LYMPHADENOPATHY; and enlargement of the liver and spleen (hepatosplenomegaly). OMIM: 312500
Date of Entry
2010/08/25
Revision Date
2019/06/18
Reticuloendotheliosis, X-linked Preferred
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