MeSH Browser

MeSH Supplementary: Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness
Unique ID: C565518
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565518
Registry Numbers: 0
Heading Mapped to: Deafness / congenital; *Hirschsprung Disease; *Hypertelorism; Kidney / abnormalities; *Polydactyly
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness MeSH Supplementary Concept Data 2025