Search on: WOLFRAM SYNDROME 
Descriptors Found: 1
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Descriptor English:   Wolfram Syndrome 
Descriptor Spanish:   Síndrome de Wolfram 
Descriptor Portuguese:   Síndrome de Wolfram 
Synonyms English:   DIDMOAD
DIDMOAD Syndrome  
Tree Number:   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
C16.131.077.951
C16.320.290.564.980
C16.320.400.630.980
C18.452.394.750.124.960
C19.246.267.960
C19.700.159.875
Definition English:   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. 
History Note English:   86 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   19570 
Unique Identifier:   D014929 

Occurrence in VHL:
 

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