- hepatic phosphorylase deficiency
- he·pat·ic phos·phor·y·lase de·fi·cien·cy (hə-patґik fos-forґə-lās) glycogen storage disease, type VI.
Medical dictionary. 2011.
Medical dictionary. 2011.
hepatic phosphorylase deficiency — glycogen storage disease, type VI … Medical dictionary
deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of … Medical dictionary
List of causes of hypoglycemia — This is a list of causes of hypoglycemia. Despite its length, it is not necessarily exhaustive, as new causes are reported regularly in the medical literature. In many individual instances of hypoglycemia, more than one contributing factor may be … Wikipedia
PHKA2 — Phosphorylase kinase, alpha 2 (liver), also known as PHKA2, is a human gene.cite web | title = Entrez Gene: PHKA2 phosphorylase kinase, alpha 2 (liver)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5256|… … Wikipedia
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
glycogenosis — Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the … Medical dictionary
Henri G. Hers — Henri Géry Hers (born 1923) is a Belgian physiologist and biochemist, and he was a professor at the Universite Catholique de Louvain. Hers disease is an inborn glycogen metabolism disorder caused by deficiency of hepatic phosphorylase, it is… … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Paroxysmal nocturnal hemoglobinuria — Classification and external resources ICD 10 D59.5 ICD 9 283.2 … Wikipedia
type IX — glycogen storage disease caused by deficiency of phosphorylase kinase; it comprises at least six different subtypes, types IXa–IXf, which vary in their mode of inheritance (either X linked or autosomal recessive) and in the tissues involved… … Medical dictionary