MeSH Browser

MeSH Supplementary: Omodysplasia type 1
Unique ID: C537746
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537746
Entry Term(s): Omodysplasia (Maroteaux); Omodysplasia 1; Omodysplasia autosomal recessive form; Omodysplasia generalized form; Omodysplasia, Autosomal Recessive; Omodysplasia, Generalized Form
Registry Number: 0
Heading Mapped to: *Growth Disorders; Osteochondrodysplasias / *congenital
Frequency: 2
Note: mutation in GPC6
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Concept UI: M0532207
Registry Number: 0
Terms: Omodysplasia type 1 Preferred Term
Term UI T743622
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Omodysplasia autosomal recessive form
Term UI T743624
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Omodysplasia, Generalized Form
Term UI T805870
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Omodysplasia 1
Term UI T805868
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Omodysplasia, Autosomal Recessive
Term UI T805869
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Omodysplasia generalized form
Term UI T743623
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Omodysplasia (Maroteaux)
Term UI T743625
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Omodysplasia type 1 MeSH Supplementary Concept Data 2024