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DIDMOAD
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DeCS
Descriptor
English
:
Wolfram Syndrome
Descriptor
Spanish
:
Síndrome de Wolfram
Descriptor
Portuguese
:
Síndrome de Wolfram
Synonyms
English
:
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:
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
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
DG
diagnostic imaging
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
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology
Record Number:
19570
Unique Identifier:
D014929
Occurrence in VHL
:
Similar:
DeCS