 Wolfram Syndrome
"Wolfram Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D014929
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| MeSH Number(s) |
C09.218.458.341.186.500.750 C10.292.700.225.500.980 C10.574.500.662.980 C10.597.751.418.341.186.500.750 C10.597.751.941.162.625.750 C11.270.564.980 C11.640.451.451.980 C11.966.075.375.750 C12.777.419.135.875 C13.351.968.419.135.875 C16.131.077.299.750 C16.320.290.564.980 C16.320.400.630.980 C18.452.394.750.124.960 C19.246.267.960 C19.700.159.875
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| Concept/Terms |
Wolfram Syndrome- Wolfram Syndrome
- Syndrome, Wolfram
- DIDMOAD
- Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness
- Wolfram Syndrome 1
- DIDMOADUD
- Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness
- DIDMOAD Syndrome
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Below are MeSH descriptors whose meaning is more general than "Wolfram Syndrome".
- Diseases [C]
- Otorhinolaryngologic Diseases [C09]
- Ear Diseases [C09.218]
- Hearing Disorders [C09.218.458]
- Hearing Loss [C09.218.458.341]
- Deafness [C09.218.458.341.186]
- Deaf-Blind Disorders [C09.218.458.341.186.500]
- Wolfram Syndrome [C09.218.458.341.186.500.750]
- Nervous System Diseases [C10]
- Cranial Nerve Diseases [C10.292]
- Optic Nerve Diseases [C10.292.700]
- Optic Atrophy [C10.292.700.225]
- Optic Atrophies, Hereditary [C10.292.700.225.500]
- Wolfram Syndrome [C10.292.700.225.500.980]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Optic Atrophies, Hereditary [C10.574.500.662]
- Wolfram Syndrome [C10.574.500.662.980]
- Neurologic Manifestations [C10.597]
- Sensation Disorders [C10.597.751]
- Hearing Disorders [C10.597.751.418]
- Hearing Loss [C10.597.751.418.341]
- Deafness [C10.597.751.418.341.186]
- Deaf-Blind Disorders [C10.597.751.418.341.186.500]
- Wolfram Syndrome [C10.597.751.418.341.186.500.750]
- Vision Disorders [C10.597.751.941]
- Blindness [C10.597.751.941.162]
- Deaf-Blind Disorders [C10.597.751.941.162.625]
- Wolfram Syndrome [C10.597.751.941.162.625.750]
- Eye Diseases [C11]
- Eye Diseases, Hereditary [C11.270]
- Optic Atrophies, Hereditary [C11.270.564]
- Wolfram Syndrome [C11.270.564.980]
- Optic Nerve Diseases [C11.640]
- Optic Atrophy [C11.640.451]
- Optic Atrophies, Hereditary [C11.640.451.451]
- Wolfram Syndrome [C11.640.451.451.980]
- Vision Disorders [C11.966]
- Blindness [C11.966.075]
- Deaf-Blind Disorders [C11.966.075.375]
- Wolfram Syndrome [C11.966.075.375.750]
- Male Urogenital Diseases [C12]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Diabetes Insipidus [C12.777.419.135]
- Wolfram Syndrome [C12.777.419.135.875]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Diabetes Insipidus [C13.351.968.419.135]
- Wolfram Syndrome [C13.351.968.419.135.875]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Abnormalities, Multiple [C16.131.077]
- Deaf-Blind Disorders [C16.131.077.299]
- Wolfram Syndrome [C16.131.077.299.750]
- Genetic Diseases, Inborn [C16.320]
- Eye Diseases, Hereditary [C16.320.290]
- Optic Atrophies, Hereditary [C16.320.290.564]
- Wolfram Syndrome [C16.320.290.564.980]
- Heredodegenerative Disorders, Nervous System [C16.320.400]
- Optic Atrophies, Hereditary [C16.320.400.630]
- Wolfram Syndrome [C16.320.400.630.980]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Glucose Metabolism Disorders [C18.452.394]
- Diabetes Mellitus [C18.452.394.750]
- Diabetes Mellitus, Type 1 [C18.452.394.750.124]
- Wolfram Syndrome [C18.452.394.750.124.960]
- Endocrine System Diseases [C19]
- Diabetes Mellitus [C19.246]
- Diabetes Mellitus, Type 1 [C19.246.267]
- Wolfram Syndrome [C19.246.267.960]
- Pituitary Diseases [C19.700]
- Diabetes Insipidus [C19.700.159]
- Wolfram Syndrome [C19.700.159.875]
Below are MeSH descriptors whose meaning is more specific than "Wolfram Syndrome".
This graph shows the total number of publications written about "Wolfram Syndrome" by people in this website by year, and whether "Wolfram Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Wolfram Syndrome" by people in Profiles.
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Rove KO, Vricella GJ, Hershey T, Thu MH, Lugar HM, Vetter J, Marshall BA, Austin PF. Lower Urinary Tract Dysfunction and Associated Pons Volume in Patients with Wolfram Syndrome. J Urol. 2018 11; 200(5):1107-1113.
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Akturk HK, Yasa S. Previously unreported abnormalities in Wolfram Syndrome Type 2. Pediatr Endocrinol Diabetes Metab. 2017; 23(2):107-110.
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Bucca BC, Klingensmith G, Bennett JL. Wolfram Syndrome: a rare optic neuropathy in youth with type 1 diabetes. Optom Vis Sci. 2011 Nov; 88(11):E1383-90.
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