MeSH Browser

MeSH Supplementary: Ribbing disease
Unique ID: C537613
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537613
Entry Term(s): Diaphyseal sclerosis, multiple; Hereditary multiple diaphyseal sclerosis; Multiple diaphyseal sclerosis
Registry Numbers: 0
Heading Mapped to: *Camurati-Engelmann Syndrome; *Osteoma, Osteoid
Frequency: 18
Note: A hereditary disorder characterized by progressive thickening and SCLEROSIS of the DIAPHYSES causing pain and swelling of lesions. In contrast to Camurati-Engelmann Syndrome, it is likely autosomal recessive in its inheritance pattern, tends to unilaterally or asymmetrically affect only the limbs, and has a later age of onset. OMIM: 601477
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Ribbing disease MeSH Supplementary Concept Data 2025