Diabetes and Deafness, Maternally Inherited (MIDD)

Alias:
Midd
Noninsulin-Dependent Diabetes Mellitus with Deafness
Diabetes-Deafness Syndrome Maternally Transmitted
Maternally-Inherited Diabetes and Hearing Loss
Maternally-Inherited Diabetes and Deafness
Maternally Inherited Diabetes and Deafness
Diabetes Mellitus, Type Ii, with Deafness
Ballinger-Wallace Syndrome
Mitochondrial Diabetes
Niddm with Deafness
Diabetes-Deafness Syndrome, Maternally Transmitted
Maternally Transmitted Diabetes-Deafness Syndrome
Mitochondrial Inherited Diabetes and Deafness
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Diabetes and Deafness, Maternally Inherited, also known as midd, is related to mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes and kearns-sayre syndrome. An important gene associated with Diabetes and Deafness, Maternally Inherited is MT-TE (Mitochondrially Encoded TRNA-Glu (GAA/G)). The drugs 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include eye and retina, and related phenotypes are constipation and type ii diabetes mellitus

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Mit
All ages
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92

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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