Search on: GANGLIOSIDOSES 
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Descriptor English:   Gangliosidoses 
Descriptor Spanish:   Gangliosidosis 
Descriptor Portuguese:   Gangliosidoses 
Tree Number:   C10.228.140.163.100.435.825.300
C16.320.565.189.435.825.300
C16.320.565.398.641.803.350
C16.320.565.595.554.825.300
C18.452.132.100.435.825.300
C18.452.584.687.803.350
C18.452.648.189.435.825.300
C18.452.648.398.641.803.350
C18.452.648.595.554.825.300
Definition English:   A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway. 
Indexing Annotation English:   coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available
History Note English:   1992(1976) 
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:   30336 
Unique Identifier:   D005733 

Occurrence in VHL:
 

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