MeSH Browser

MeSH Supplementary: Wolfram Syndrome, Mitochondrial Form
Unique ID: C564012
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564012
Entry Term(s): DIDMOAD Syndrome, Mitochondrial Form; Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness, Mitochondrial Form
Registry Numbers: 0
Heading Mapped to: *Diabetes Insipidus; *Diabetes Mellitus; *Hearing Loss, Sensorineural; *Optic Atrophies, Hereditary
Frequency: 1
Note: PROM mutation in WFS1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Wolfram Syndrome, Mitochondrial Form MeSH Supplementary Concept Data 2025