Search on: GLYCOGEN STORAGE DISEASE TYPE VII 
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Descriptor English:   Glycogen Storage Disease Type VII 
Descriptor Spanish:   Enfermedad del Almacenamiento de Glucógeno Tipo VII 
Descriptor Portuguese:   Doença de Depósito de Glicogênio Tipo VII 
Synonyms English:   Glycogenosis 7
Tarui Disease  
Tree Number:   C05.651.534.500.149
C16.320.565.202.449.600
C16.320.577.149
C18.452.648.202.449.600
Definition English:   An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant. 
Indexing Annotation English:   do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
History Note English:   91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 7 see under GLYCOGENOSIS 1975-88 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Record Number:   24397 
Unique Identifier:   D006014 

Occurrence in VHL:
 

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