MeSH Browser

MeSH Supplementary: Robinson Miller Bensimon syndrome
Unique ID: C535864
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535864
Entry Term(s): Deafness and onychodystrophy, dominant form
Registry Numbers: 0
Heading Mapped to: *Ectodermal Dysplasia; *Hearing Loss, Sensorineural
Frequency: 0
Note: Familial ectodermal dysplasia with sensori-neural deafness and other anomalies
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Robinson Miller Bensimon syndrome MeSH Supplementary Concept Data 2025