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Multifocal fibrosclerosis MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
Retroperitoneal Fibrosis / *congenital
Frequency
20
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 Preferred
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