| Descriptor English: | Wolfram Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Wolfram
| ||||||
| Descriptor Portuguese: | Síndrome de Wolfram | ||||||
| Descriptor French: | Syndrome de Wolfram | ||||||
| Entry term(s): |
DIDMOAD DIDMOAD Syndrome DIDMOADUD Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness Syndrome, Wolfram Wolfram Syndrome 1 |
||||||
| Tree 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 C12.050.351.968.419.135.875 C12.200.777.419.135.875 C12.950.419.135.875 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 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D014929 | ||||||
| Scope note: | 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. |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Previous Indexing: |
Deafness (1966-1985) Diabetes Insipidus (1966-1985) Diabetes Mellitus, Insulin-Dependent (1984-1985) Optic Atrophy (1966-1985) |
||||||
| Public MeSH Note: | 86 |
||||||
| History Note: | 86 |
||||||
| DeCS ID: | 19570 | ||||||
| Unique ID: | D014929 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1986/01/01 | ||||||
| Date of Entry: | 1985/03/11 | ||||||
| Revision Date: | 2019/07/05 |
-
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
|
|
Wolfram Syndrome
- Preferred
Wolfram Syndrome 1
- Narrower
| Concept UI |
M0022993 |
| Scope note | 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. |
| Preferred term | Wolfram Syndrome |
| Entry term(s) |
DIDMOAD DIDMOAD Syndrome DIDMOADUD Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness Syndrome, Wolfram |
| Concept UI |
M000648357 |
| Preferred term | Wolfram Syndrome 1 |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
