MeSH Browser

MeSH Heading: Glycogen Storage Disease Type VI
Tree Number(s): C16.320.565.202.449.580; C18.452.648.202.449.580
Unique ID: D006013
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006013
Scope Note: A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.
Entry Version: GLYCOGEN STORAGE DIS VI
Entry Term(s): Glycogenosis 6; Glycogenosis Type VI; Glycogenosis VI; Hepatic Glycogen Phosphorylase Deficiency; Hers Disease; Hers' Disease; Liver Phosphorylase Deficiency Syndrome
Previous Indexing: Glucosyltransferases/metabolism (1966-1974); Glycogenosis (1966-1974); Liver Diseases (1966-1974)
See Also: Glycogen Phosphorylase, Liver Form
Public MeSH Note: 91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 6 see under GLYCOGENOSIS 1975-88
Online Note: use GLYCOGEN STORAGE DISEASE TYPE VI to search GLYCOGENOSIS 6 1975-88
History Note: 91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 6 see under GLYCOGENOSIS 1975-88
Date Established: 1991/01/01
Date of Entry: 1974/12/12
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Glycogen Storage Disease Type VI MeSH Descriptor Data 2025