MeSH Browser

MeSH Supplementary: Reticuloendotheliosis, X-linked
Unique ID: C538362
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538362
Entry Term(s): Reticuloendotheliosis
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 MeSH Supplementary Concept Data 2024