MeSH Browser

MeSH Supplementary: Hirschsprung disease 1
Unique ID: C538540
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538540
Entry Term(s): Hirschsprung disease type 1
Registry Numbers: 0
Heading Mapped to: *Hirschsprung Disease
Frequency: 289
Note: A hereditary form of Hirschsprung Disease associated with mutations in the RET gene. OMIM: 142623
Date of Entry: 2010/08/25
Revision Date: 2016/07/11

Hirschsprung disease 1 MeSH Supplementary Concept Data 2025