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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 / DIDMOAD Syndrome / Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness / Syndrome, Wolfram /
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Wolfram Syndrome"
             

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Broader term(s): - Deaf-Blind Disorders - Deafness - Hearing Loss - Hearing Disorders - Ear Diseases - Otorhinolaryngologic Diseases - Optic Atrophies, Hereditary - Optic Atrophy - Optic Nerve Diseases - Cranial Nerve Diseases - Nervous System Diseases - Diabetes Insipidus - Kidney Diseases - Urologic Diseases - Male Urogenital Diseases - Abnormalities, Multiple - Congenital Abnormalities - Congenital, Hereditary, and Neonatal Diseases and Abnormalities - Diabetes Mellitus, Type 1 - Diabetes Mellitus - Metabolic Diseases

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  Medical image(s) for "Wolfram Syndrome"
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Broader term(s): - Hearing Loss - Nervous System Diseases - Kidney Diseases - Diabetes Mellitus
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  Medical News for "Wolfram Syndrome"
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Broader term(s): - Hearing Disorders - Ear Diseases - Nervous System Diseases - Congenital 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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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 
              Congenital Abnormalities
                  Abnormalities, Multiple 
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Congenital Abnormalities
                  Abnormalities, Multiple
                      Deaf-Blind Disorders 
      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
              Vision Disorders
                  Blindness
                      Deaf-Blind Disorders 
              Optic Nerve Diseases
                  Optic Atrophy
                      Optic Atrophies, Hereditary 
              Eye Diseases, Hereditary
                  Optic Atrophies, Hereditary 
      Diseases
          Nervous System Diseases
              Neurologic Manifestations
                  Sensation Disorders
                      Vision Disorders
                          Blindness
                              Deaf-Blind Disorders 
                      Hearing Disorders
                          Hearing Loss
                              Deafness
                                  Deaf-Blind Disorders 
              Neurodegenerative Diseases
                  Heredodegenerative Disorders, Nervous System
                      Optic Atrophies, Hereditary 
      Diseases
          Nervous System Diseases
              Cranial Nerve Diseases
                  Optic Nerve Diseases
                      Optic Atrophy
                          Optic Atrophies, Hereditary 
      Diseases
          Otorhinolaryngologic Diseases
              Ear Diseases
                  Hearing Disorders
                      Hearing Loss
                          Deafness
                              Deaf-Blind Disorders 

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

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