MeSH Browser

MeSH Supplementary: Acrorenal syndrome recessive
Unique ID: C535666
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535666
Entry Term(s): Acrorenal Syndrome, Autosomal Recessive; Acrorenal syndrome autosomal recessive; Curran syndrome
Registry Number: 0
Heading Mapped to: *Digestive System Abnormalities; *Limb Deformities, Congenital
Frequency: 0
Date of Entry: 2010/06/25
Revision Date: 2012/12/04

Concept UI: M0530127
Registry Number: 0
Terms: Acrorenal syndrome recessive Preferred Term
Term UI T736818
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Acrorenal Syndrome, Autosomal Recessive
Term UI T807720
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Acrorenal syndrome autosomal recessive
Term UI T736819
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Curran syndrome
Term UI T736820
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Acrorenal syndrome recessive MeSH Supplementary Concept Data 2023