MeSH Browser

MeSH Supplementary: Santos Mateus Leal syndrome
Unique ID: C537235
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537235
Entry Term(s): Hirschsprung disease, deafness and polydactyly
Registry Numbers: 0
Heading Mapped to: *Hearing Loss, Central; *Hirschsprung Disease; *Hypertelorism; *Polydactyly
Frequency: 0
Note: Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Santos Mateus Leal syndrome MeSH Supplementary Concept Data 2025