MeSH Browser

MeSH Supplementary: Multifocal fibrosclerosis
Unique ID: C537375
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537375
Entry Term(s): Fibrosclerosis, Multifocal; Mediastinal fibrosis, familial; Retroperitoneal fibrosis, familial
Registry Numbers: 0
Heading Mapped to: Retroperitoneal Fibrosis / congenital
Frequency: 21
Note: A hereditary autosomal recessive connective tissue disorder characterized by retroperitoneal fibrosis, Riedel sclerosing THYROIDITIS; SCLEROSING CHOLANGITIS; ORBITAL PSEUDOTUMOR, seronegative SPONDYLARTHROPATHY; finger CONTRACTURES, camptodactyly, and mediastinal fibrosis. OMIM: 228800
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Multifocal fibrosclerosis MeSH Supplementary Concept Data 2025