MeSH Browser

MeSH Supplementary: Noninsulin-dependent diabetes mellitus with deafness
Unique ID: C536246
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536246
Entry Term(s): Ballinger-Wallace Syndrome; Diabetes Mellitus, Type II, With Deafness; Diabetes and deafness, maternally inherited; Diabetes mellitus, type 2, with deafness; Diabetes-deafness syndrome, maternally transmitted; Maternally Transmitted Diabetes-Deafness Syndrome; Maternally inherited diabetes and deafness; Mitochondrial Inherited Diabetes and Deafness; NIDDM with deafness
Heading Mapped to: *Deafness; *Diabetes Mellitus, Type 2; *Mitochondrial Diseases
Frequency: 88
Note: A mitochondrial disorder characterized by onset of SENSORINEURAL HEARING LOSS and diabetes in adulthood. Some patients may have additional features observed in mitochondrial disorders, including RETINITIS PIGMENTOSA; PTOSIS; CARDIOMYOPATHY; MUSCULAR DISEASES; KIDNEY DISEASES, and neuropsychiatric symptoms. Mutations in the MITOCHONDRIAL GENES MTTL1, MTTE, and MTTK have been identified. OMIM: 520000
Date of Entry: 2010/11/13
Revision Date: 2015/08/18

Noninsulin-dependent diabetes mellitus with deafness MeSH Supplementary Concept Data 2024