| Descriptor English: | Gangliosidoses | ||||
| Descriptor Spanish: |
Gangliosidosis
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| Descriptor Portuguese: | Gangliosidoses | ||||
| Descriptor French: | Gangliosidoses | ||||
| Entry term(s): |
Ganglioside Storage Disease Ganglioside Storage Diseases Ganglioside Storage Disorder Ganglioside Storage Disorders Gangliosidosis Storage Disease, Ganglioside Storage Diseases, Ganglioside Storage Disorder, Ganglioside Storage Disorders, Ganglioside |
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| Tree number(s): |
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 C18.452.584.563.641.803.350 C18.452.648.189.435.825.300 C18.452.648.398.641.803.350 C18.452.648.595.554.825.300 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005733 | ||||
| Scope note: | 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. |
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| Annotation: | coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Gangliosides (1966-1975) Lipoidosis (1966-1975) |
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| Public MeSH Note: | 1992; see GANGLIOSIDOSIS 1976-91 |
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| History Note: | 1992(1976) |
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| Related: |
Mucolipidoses
MeSH | ||||
| DeCS ID: | 30336 | ||||
| Unique ID: | D005733 | ||||
| NLM Classification: | WD 205.5.L5 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1976/01/01 | ||||
| Date of Entry: | 1975/07/23 | ||||
| Revision Date: | 2010/06/25 |
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Gangliosidoses
- Preferred
| Concept UI |
M0008988 |
| Scope note | 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. |
| Preferred term | Gangliosidoses |
| Entry term(s) |
Ganglioside Storage Disease Ganglioside Storage Diseases Ganglioside Storage Disorder Ganglioside Storage Disorders Gangliosidosis Storage Disease, Ganglioside Storage Diseases, Ganglioside Storage Disorder, Ganglioside Storage Disorders, Ganglioside |
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