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751 Possible Causes for Phosphoglycerate Kinase Deficiency

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms.[biomedsearch.com] Synonyms: Phosphoglycerokinase deficiency, PGK deficiency, PGK1 deficiency, Haemolytic anaemia with PGK Deficiency, Phosphoglycerate kinase deficiency is a hereditary metabolic[patient.info] PGK deficiency PGK1 deficiency phosphoglycerate kinase 1 deficiency Aasly J, van Diggelen OP, Boer AM, Brønstad G.[ghr.nlm.nih.gov]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Glycogen storage disease due to phosphoglycerate mutase deficiency Glycogen storage disease[familydiagnosis.com] storage disease due to phosphoglycerate kinase 1 deficiency Pelizaeus-Merzbacher-like due to HSPD1 mutation Synonym(s): - GSD due to aldolase A deficiency - GSD type 12 -[csbg.cnb.csic.es] deficiency, phosphoglycerate kinase deficiency, phosphoglycerate mutase deficiency, Tarui disease, and GSD.[medlink.com]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Glycogen storage disease due to phosphoglycerate mutase deficiency Glycogen storage disease[familydiagnosis.com] deficiency, phosphoglycerate kinase deficiency, phosphoglycerate mutase deficiency, Tarui disease, and GSD.[medlink.com] We observed an interesting as- sociation between phosphoglycerate kinase deficiency (GSD IX) and juvenile Parkinsonism, which is probably causal rather than casual.[archive.org]

  • Glycogen Storage Disease Type 9

    Phosphoglycerate Kinase Deficiency 2018-06-29T12:50:23 00:00 What is Phosphoglycerate kinase deficiency (PGK deficiency)?[mda.org.au] Phosphoglycerate kinase deficiency What is phosphoglycerate kinase deficiency (glycogenosis type 9)?[mda.org] deficiency, phosphoglycerate kinase deficiency, phosphoglycerate mutase deficiency, Tarui disease, and GSD.[medlink.com]

  • Genetic Recurrent Myoglobinuria

    kinase deficiency (311800), the attacks in recurrent myoglobinuria no relation to exercise, but are triggered by intercurrent illnesses, commonly upper respiratory tract[ncbi.nlm.nih.gov] Unlike the exercise-induced rhabdomyolyses such as McArdle syndrome (232600), carnitine palmitoyltransferase deficiency (see 255110), and the Creteil variety of phosphoglycerate[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease due to GLUT2 Deficiency

    deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Glycogen storage disease due to phosphoglycerate mutase deficiency Glycogen storage disease[familydiagnosis.com] 70 glycogenosis X (phosphoglycerate mutase deficiency) 71 phosphoglycerate kinase deficiency 72 lactate dehydrogenase deficiency (type XI) 73 aldolase A deficiency (type[boks.be] 2012-10-01 Phosphoglycerate kinase deficiency and phosphoglycerate mutase deficiency Darras BT, Craigen WJ UpToDate, Wolters Kluwer Health - 2012-10-23 Phosphorylase b kinase[doximity.com]

  • Prata-Libéral-Gonçalves Syndrome

    deficiency type 2 Phosphoglucomutase deficiency type 3 Phosphoglucomutase deficiency type 4 Phosphoglycerate kinase 1 deficiency Phosphoglycerate kinase deficiency Phosphomannoisomerase[mindmappedia.com] deficiency type 3 Phosphoglucomutase deficiency type 4 Phosphoglucomutase deficiency Phosphoglycerate kinase 1 deficiency Phosphoglycerate kinase deficiency Phosphomannoisomerase[bioreference.net] Phosphoglucomutase deficiency[?] Phosphoglycerate kinase 1 deficiency[?] Phosphoglycerate kinase deficiency[?] Phosphomannoisomerase deficiency[?][encyclopedia.kids.net.au]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    HMOX1 HS type 1 HS type 2 HS type 3 HS type 4 HS type 5 KIF23 KLF1 NT5C3A Ovalocytosis P5NT PFK PFKM PGK PGK1 Phosphofructose kinase deficiency Phosphoglycerate kinase 1[mayomedicallaboratories.com] Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency[icd9data.com] Phosphoglycerate kinase deficiency is an XL disease due to mutations of Xq13.[cancertherapyadvisor.com]

  • X-linked Parkinsonism-Spasticity Syndrome

    471 Phosphoglycerate Kinase Deficiency 489 1 508 ArnoldChiari Syndrome 515 Tuberous Sclerosis 595 23 602 Muscular Dystrophy Becker 621 Neuromyotonia 635 20 659 Usher Syndrome[books.google.com] Sheehan Syndrome 328 EMERGINGINFECTIOUS 30 Thyroiditis Chronic Lymphocytic DISEASES 277 31 ZollingerEllison Syndrome 330 11 368 Lynch Syndromes 401 16 430 Homocystinuria 459 Deficiency[books.google.com]

  • Autosomal Dominant Myoglobinuria

    kinase deficiency (311800), the attacks in recurrent myoglobinuria no relation to exercise, but are triggered by intercurrent illnesses, commonly upper respiratory tract[ncbi.nlm.nih.gov] kinase deficiency ({311800}), the attacks in recurrent myoglobinuria no relation to exercise, but are triggered by intercurrent illnesses, commonly upper respiratory tract[diseaseinfosearch.org] Unlike the exercise-induced rhabdomyolyses such as McArdle syndrome (232600), carnitine palmitoyltransferase deficiency (see 255110), and the Creteil variety of phosphoglycerate[ncbi.nlm.nih.gov]

Further symptoms