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Wolfram Syndrome
Definition: A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.

Synonym(s): DIDMOAD / Syndrome, Wolfram /
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Wolfram Syndrome"
             

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info: enter the site: (click below) domain of the site:  
view the HON description of the site HONcode - children with DIABETES - DIDMOAD (Wolfram Syndrome)www.childrenwithdiabetes.com 4
view the HON description of the site HONcode - WFS1 - Wolfram syndrome 1 (wolframin) - Genetics Home Referenceghr.nlm.nih.gov  
view the HON description of the site HONcode - Orphanet: Wolfram syndromewww.orpha.net 2
view the robot description of the site rare-diseases — National Organization for Rare Disorderswww.rarediseases.org  
 
 

Broader term(s): - Optic Atrophies, Hereditary - Optic Atrophy - Optic Nerve Diseases - Cranial Nerve Diseases - Nervous System Diseases - Diabetes Insipidus - Kidney Diseases - Urologic Diseases - Abnormalities, Multiple - Abnormalities - Congenital, Hereditary, and Neonatal Diseases and Abnormalities - Diabetes Mellitus, Type 1 - Diabetes Mellitus - Metabolic Diseases - Nutritional and Metabolic Diseases

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  Medical image(s) for "Wolfram Syndrome"
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Broader term(s): - Nervous System Diseases - Kidney Diseases - Diabetes Mellitus, Type 1 - Diabetes Mellitus
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  Medical News for "Wolfram Syndrome"
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Broader term(s): - Nervous System Diseases - Abnormalities

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  Scientific articles from MEDLINE for "Wolfram Syndrome"
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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy

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  Clinical Trials for "Wolfram Syndrome"
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Broader term(s): - Optic Atrophy - Optic Nerve Diseases - Nervous System Diseases - Diabetes Insipidus - Kidney Diseases - Urologic Diseases - Abnormalities - Congenital, Hereditary, and Neonatal Diseases and Abnormalities - Diabetes Mellitus, Type 1 - Diabetes Mellitus - Glucose Metabolism Disorders - Metabolic Diseases

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  Medical Conferences/Events for "Wolfram Syndrome"
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Broader term(s): - Diabetes Mellitus

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy


  Broader term(s):
      Diseases
          Endocrine System Diseases
              Pituitary Diseases
                  Diabetes Insipidus 
              Diabetes Mellitus
                  Diabetes Mellitus, Type 1 
      Diseases
          Nutritional and Metabolic Diseases
              Metabolic Diseases
                  Glucose Metabolism Disorders
                      Diabetes Mellitus
                          Diabetes Mellitus, Type 1 
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Heredodegenerative Disorders, Nervous System
                      Optic Atrophies, Hereditary 
                  Eye Diseases, Hereditary
                      Optic Atrophies, Hereditary 
              Abnormalities
                  Abnormalities, Multiple 
      Diseases
          Female Urogenital Diseases and Pregnancy Complications
              Female Urogenital Diseases
                  Urologic Diseases
                      Kidney Diseases
                          Diabetes Insipidus 
      Diseases
          Male Urogenital Diseases
              Urologic Diseases
                  Kidney Diseases
                      Diabetes Insipidus 
      Diseases
          Eye Diseases
              Optic Nerve Diseases
                  Optic Atrophy
                      Optic Atrophies, Hereditary 
              Eye Diseases, Hereditary
                  Optic Atrophies, Hereditary 
      Diseases
          Nervous System Diseases
              Neurodegenerative Diseases
                  Heredodegenerative Disorders, Nervous System
                      Optic Atrophies, Hereditary 
              Cranial Nerve Diseases
                  Optic Nerve Diseases
                      Optic Atrophy
                          Optic Atrophies, Hereditary 

MeSH 2010 © U.S. National Library of Medicine®.

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