MeSH Browser

MeSH Supplementary: Waardenburg Syndrome, Type 4c
Unique ID: C567679
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567679
Entry Term(s): Waardenburg Syndrome With Hirschsprung Disease, Type 4c Waardenburg Syndrome, Type Ivc
Registry Numbers: 0
Heading Mapped to: *Hirschsprung Disease; *Waardenburg Syndrome; SOXE Transcription Factors / deficiency
Frequency: 0
Note: mutations in SOX10
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Waardenburg Syndrome, Type 4c MeSH Supplementary Concept Data 2025