MeSH Browser

MeSH Supplementary: Konigsmark Knox Hussels syndrome
Unique ID: C537214
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537214
Entry Term(s): Deafness optic atrophy syndrome; Dominant congenital deafness and progressive optic nerve atrophy
Registry Numbers: 0
Heading Mapped to: *Deafness; *Optic Atrophies, Hereditary
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2010/08/25

Konigsmark Knox Hussels syndrome MeSH Supplementary Concept Data 2025