| Descriptor English: | Glycogen Storage Disease Type VIII | ||||||
| Descriptor Spanish: |
Enfermedad del Almacenamiento de Glucógeno Tipo VIII
| ||||||
| Descriptor Portuguese: | Doença de Depósito de Glicogênio Tipo VIII | ||||||
| Descriptor French: | Glycogénose de type VIII | ||||||
| Entry term(s): |
Glycogenosis 8 |
||||||
| Tree number(s): |
C16.320.322.217 C16.320.565.202.449.620 C18.452.648.202.449.620 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006015 | ||||||
| Scope note: | An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon. |
||||||
| Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
||||||
| 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 |
||||||
| Previous Indexing: |
Glycogenosis (1966-1974) |
||||||
| Public MeSH Note: | 91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 8 see under GLYCOGENOSIS 1975-88 |
||||||
| Online Note: | use GLYCOGEN STORAGE DISEASE TYPE VIII to search GLYCOGENOSIS 8 1975-88 |
||||||
| History Note: | 91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 8 see under GLYCOGENOSIS 1975-88 |
||||||
| Entry Version: | GLYCOGEN STORAGE DIS VIII |
||||||
| DeCS ID: | 24398 | ||||||
| Unique ID: | D006015 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1974/12/12 | ||||||
| Revision Date: | 2006/07/05 |
|
|
Glycogen Storage Disease Type VIII
- Preferred
| Concept UI |
M0009476 |
| Scope note | An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon. |
| Preferred term | Glycogen Storage Disease Type VIII |
| Entry term(s) |
Glycogenosis 8 |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
