MeSH Browser

MeSH Supplementary: Sprengel deformity
Unique ID: C535802
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535802
Entry Term(s): High scapula; Maladie de Sprengel familiale; Sprengel's shoulder
Registry Number: 0
Heading Mapped to: *Congenital Abnormalities; Scapula / *abnormalities; Shoulder Joint / *abnormalities
Frequency: 71
Note: A congenital condition where one or both shoulder blades (scapula) are underdeveloped and abnormally high placed. There may also be anomalies of the bone and soft tissues in the shoulder girdle, as well as the ribs and spine. It is caused by the failure of descent of the shoulder blades during fetal development and is more common in females. The condition is usually sporadic; familial cases appear to be autosomal dominant. OMIM:184400
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Concept UI: M0530263
Registry Number: 0
Terms: Sprengel deformity Preferred Term
Term UI T737271
Date02/24/2009
LexicalTag NON
ThesaurusID; Maladie de Sprengel familiale
Term UI T737274
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Sprengel's shoulder
Term UI T737275
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); High scapula
Term UI T737273
Date02/24/2009
LexicalTag NON
ThesaurusID

Sprengel deformity MeSH Supplementary Concept Data 2024