- myophosphorylase deficiency
- myo·phos·phor·y·lase de·fi·cien·cy (mi″o-fos-forґə-lās) glycogen storage disease, type V.
Medical dictionary. 2011.
Medical dictionary. 2011.
myophosphorylase deficiency glycogenosis — glycogen storage disease, type V … Medical dictionary
Myophosphorylase — phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V) Myophosphorylase … Wikipedia
Glycogen storage disease type V — Classification and external resources ICD 10 E74.0 ICD 9 271.0 … Wikipedia
Morbus McArdle — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit … Deutsch 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
McArdle-Krankheit — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit … Deutsch Wikipedia
McArdle-Syndrom — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit … Deutsch Wikipedia
List of diseases (M) — A list of diseases in the English wikipedia.DiseasesTOC MaMac* Mac Ardle disease * Mac Dermot Patton Williams syndrome * Mac Dermot Winter syndromeMaci Macr* Macias Flores Garcia Cruz Rivera syndrome * Mackay Shek Carr syndrome * Macleod Fraser… … Wikipedia
McArdle's disease — McArdle s disease, McBurney s point see entries alphabetized as MC Mc·Ar·dle s disease mək ärd əlz n glycogen storage disease that is inherited as an autosomal recessive trait, is marked esp. by muscle weakness and myoglobinuria, and is caused by … Medical dictionary
McArdle's disease — noun Glycogen storage disease type V, a metabolic disorder caused by a deficiency of myophosphorylase … Wiktionary