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AMYOTONIA CONGENITA
Descriptors Found:
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DeCS
Descriptor
English
:
Neuromuscular Diseases
Descriptor
Spanish
:
Enfermedades Neuromusculares
Descriptor
Portuguese
:
Doenças Neuromusculares
Synonyms
English
:
Amyotonia Congenita
Oppenheim Disease
Tree Number:
C10.668
Definition
English
:
A general term encompassing lower
MOTOR NEURON DISEASE
;
PERIPHERAL NERVOUS SYSTEM DISEASES
; and certain
MUSCULAR DISEASES
. Manifestations include
MUSCLE WEAKNESS
;
FASCICULATION
; muscle
ATROPHY
; SPASM;
MYOKYMIA
;
MUSCLE HYPERTONIA
, myalgias, and
MUSCLE HYPOTONIA.
Indexing Annotation
English
:
GEN; do not confuse xref AMYOTONIA CONGENITA with
MYOTONIA CONGENITA
History Note
English
:
1971; AMYOTONIA CONGENITA was heading 1963-96
Allowable Qualifiers
English
:
BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
CN
congenital
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:
9660
Unique Identifier:
D009468
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
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