5.4.2.2 Abortion, Spontaneous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1340043&form=6&db=m Phosphoglucomutase genetic polymorphism and human fertility. therapeutic application,unassigned 1,0 5.4.2.2 Abortion, Spontaneous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6131042&form=6&db=m Genetic polymorphisms and human reproduction: a study of phosphoglucomutase in spontaneous abortion. diagnostic usage,ongoing research,unassigned 3,4,0 5.4.2.2 Abortion, Spontaneous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11466970&form=6&db=m Phosphoglucomutase genetic polymorphism of newborns. causal interaction,unassigned 3,0 5.4.2.2 Adenocarcinoma of Lung http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32855723&form=6&db=m Identification of key differentially expressed mRNAs and microRNAs in non-small cell lung cancer using bioinformatics analysis. causal interaction,diagnostic usage,ongoing research,unassigned 1,4,3,0 5.4.2.2 Agammaglobulinemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34261177&form=6&db=m Common Variable Immunodeficiency and Other Immunodeficiency Syndromes in Bronchiectasis. causal interaction,unassigned 4,0 5.4.2.2 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13605990&form=6&db=m [Erythrocyte enzymes; activity of glycolytic enzymes of erythrocytes in anemia: phosphoglucomutase, phosphohexoisomerase, diphosphofructaldolase, lactic acid dehydrogenase.] ongoing research,unassigned 1,0 5.4.2.2 Anemia, Hemolytic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13811376&form=6&db=m [Enzymatic activity of glycolysis in the erythrocytes in the course of an experimental hemolytic anemia: phosphoglucomutase, aldolase and enolase activity.] ongoing research,unassigned 2,0 5.4.2.2 Asthma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12096683&form=6&db=m Genetic-biochemical criteria for individual sensitivity in development of occupational bronchopulmonary diseases. unassigned - 5.4.2.2 Ataxia Telangiectasia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29943473&form=6&db=m Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran. causal interaction,diagnostic usage,unassigned 4,4,0 5.4.2.2 Autoimmune Lymphoproliferative Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Breast Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33986801&form=6&db=m miR-1224-3p Promotes Breast Cancer Cell Proliferation and Migration through PGM5-Mediated Aerobic Glycolysis. ongoing research,unassigned 1,0 5.4.2.2 Bronchiectasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34261177&form=6&db=m Common Variable Immunodeficiency and Other Immunodeficiency Syndromes in Bronchiectasis. causal interaction,unassigned 4,0 5.4.2.2 Bronchitis, Chronic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12096683&form=6&db=m Genetic-biochemical criteria for individual sensitivity in development of occupational bronchopulmonary diseases. unassigned - 5.4.2.2 Carcinogenesis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=826019&form=6&db=m [Glycogen and enzymes involved in its biosynthesis in rat liver during liver carcinogenesis caused by diethylnitrosamine] ongoing research,unassigned 1,0 5.4.2.2 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3810899&form=6&db=m [Characteristics of hexosephosphate transformation regulation in Zajdela hepatoma and the liver of tumor-bearing rats] causal interaction,unassigned 1,0 5.4.2.2 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30335765&form=6&db=m Phosphoglucomutase 1 inhibits hepatocellular carcinoma progression by regulating glucose trafficking. causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 5.4.2.2 Cardiomyopathy, Dilated http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19377068&form=6&db=m Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy. causal interaction,unassigned 3,0 5.4.2.2 Cardiomyopathy, Dilated http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26303607&form=6&db=m News on Clinical Details and Treatment in PGM1-CDG. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Chagas Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=407674&form=6&db=m The identification by isoenzyme patterns of two distinct strain-groups of Trypanosoma cruzi, circulating independently in a rural area of Brazil. diagnostic usage,ongoing research,unassigned 3,2,0 5.4.2.2 Chordoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2287590&form=6&db=m The nature of cytoplasmic vacuoles in chordoma cells. A correlative enzyme and electron microscopic histochemical study. unassigned - 5.4.2.2 Choriocarcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1115169&form=6&db=m Enzymes of normal and malignant trophoblast: phosphoglucose isomerase, phosphoglucomutase, hexokinase, lactate dehydrogenase, and alkaline phosphatase. causal interaction,ongoing research,unassigned 1,3,0 5.4.2.2 Coccidiosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1836082&form=6&db=m [Histochemistry of nucleoside phosphatases and phosphoglucomutase in the small intestine during coccidiosis in piglets] ongoing research,unassigned 2,0 5.4.2.2 Common Variable Immunodeficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34261177&form=6&db=m Common Variable Immunodeficiency and Other Immunodeficiency Syndromes in Bronchiectasis. causal interaction,unassigned 4,0 5.4.2.2 Congenital Disorders of Glycosylation http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26303607&form=6&db=m News on Clinical Details and Treatment in PGM1-CDG. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22976764&form=6&db=m A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26303607&form=6&db=m News on Clinical Details and Treatment in PGM1-CDG. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27351072&form=6&db=m PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure. causal interaction,unassigned 4,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28794993&form=6&db=m Limitations of galactose therapy in phosphoglucomutase 1 deficiency. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30048639&form=6&db=m Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency. causal interaction,unassigned 4,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31077402&form=6&db=m A novel phosphoglucomutase-deficient mouse model reveals aberrant glycosylation and early embryonic lethality. causal interaction,unassigned 3,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33342467&form=6&db=m Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots. causal interaction,unassigned 2,0 5.4.2.2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33534079&form=6&db=m Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations. causal interaction,diagnostic usage,therapeutic application,unassigned 4,4,1,0 5.4.2.2 Cystic Fibrosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6449826&form=6&db=m Duffy blood group system, phosphoglucomutase and glutamate-pyruvate transminase in homo- and heterozygous cases of mucoviscidosis. causal interaction,diagnostic usage,ongoing research,therapeutic application 1,3,2,2 5.4.2.2 Cysts http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1829658&form=6&db=m [Distribution of zymodemes of Entamoeba histolytica from different areas of China] ongoing research,unassigned 1,0 5.4.2.2 Dermatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Diabetes Mellitus, Experimental http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=704561&form=6&db=m [UDPG pyrophosphorylase and phosphoglucomutase activity in the liver of rats with alloxan diabetes] ongoing research,unassigned 3,0 5.4.2.2 Diabetes Mellitus, Type 1 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7791012&form=6&db=m Genetic and non genetic factors in the outcome of diabetic pregnancy. unassigned - 5.4.2.2 Down Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=126209&form=6&db=m Types of enzymatic overdosing in trisomy 21: erythrocytic superoxide dismutase-AJ and phosphoglucomutase. unassigned - 5.4.2.2 Dysentery, Amebic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1829658&form=6&db=m [Distribution of zymodemes of Entamoeba histolytica from different areas of China] ongoing research,unassigned 1,0 5.4.2.2 Dyslipidemias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22708969&form=6&db=m Diabetogenic effects of Parthinium hysterophorous induced allergic rhinitis. diagnostic usage,unassigned 2,0 5.4.2.2 Eczema http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33534079&form=6&db=m Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations. causal interaction,diagnostic usage,therapeutic application,unassigned 4,4,1,0 5.4.2.2 Endometrial Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=508567&form=6&db=m Isoenzymes of hexokinase, 6-phosphogluconate dehydrogenase, phosphoglucomutase and lactate dehydrogenase in uterine cancer. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 5.4.2.2 Endometriosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9102363&form=6&db=m [Genetic aspects of endometriosis: features of the distribution of polymorphic gene frequencies] diagnostic usage,ongoing research,unassigned 2,1,0 5.4.2.2 Ependymoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17340808&form=6&db=m [Histochemical demonstration of glial enzyme activity. II. Reagent and neoplastic glia] causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Essential Hypertension http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2742764&form=6&db=m [Genetic markers and susceptibility to hypertension] diagnostic usage,ongoing research,unassigned 2,2,0 5.4.2.2 Fetal Macrosomia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7791012&form=6&db=m Genetic and non genetic factors in the outcome of diabetic pregnancy. unassigned - 5.4.2.2 Fetal Macrosomia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8863716&form=6&db=m On the association between maternal phosphoglucomutase 1 (PGM1) and fetal macrosomia in diabetic pregnancy. causal interaction,unassigned 1,0 5.4.2.2 Galactosemias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1476788&form=6&db=m Minimizing false positive diagnoses in newborn screening for galactosemia. diagnostic usage,ongoing research,unassigned 1,2,0 5.4.2.2 Galactosemias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6213094&form=6&db=m [Hereditary galactosemia in rats: biochemical mechanisms of the disease] diagnostic usage,unassigned 3,0 5.4.2.2 Galactosemias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6452554&form=6&db=m [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)] causal interaction,unassigned 4,0 5.4.2.2 Galactosemias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7200438&form=6&db=m [Biochemical mechanisms of the development of hereditary galactosemia in W/SSM strain rats] diagnostic usage,unassigned 3,0 5.4.2.2 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32681750&form=6&db=m International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): Diagnosis, follow-up, and management. causal interaction,diagnostic usage,unassigned 4,2,0 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2965317&form=6&db=m Infantile muscle glycogen storage disease: phosphoglucomutase deficiency with decreased muscle and serum carnitine levels. causal interaction,diagnostic usage,unassigned 4,1,0 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19625727&form=6&db=m Muscle glycogenosis due to phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22976764&form=6&db=m A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27351072&form=6&db=m PGM1 deficiency diagnosed during an endocrine work-up of low IGF-1 mediated growth failure. causal interaction,unassigned 4,0 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28794993&form=6&db=m Limitations of galactose therapy in phosphoglucomutase 1 deficiency. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Glycogen Storage Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29752652&form=6&db=m Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion. causal interaction,unassigned 4,0 5.4.2.2 Hematologic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13811377&form=6&db=m [Observations on the behavior of erythrocytic phosphoglucomutase activity in patients with neoplasms and malignant blood diseases.] diagnostic usage,ongoing research,unassigned 3,2,0 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13414774&form=6&db=m Serum phosphoglucomutase activity in human virus hepatitis. diagnostic usage,ongoing research,unassigned 4,4,0 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13446128&form=6&db=m [Recent research on the enzymatic activity of the liver and blood in experimental MHV-3 virus hepatitis: adenylpyrophosphatase, succinic dehydrogenase, rhodanese and phosphoglucomutase.] ongoing research,therapeutic application,unassigned 3,1,0 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13451339&form=6&db=m [Phosphoglucomutase activity of blood in human viral hepatitis and in other icterogenic liver diseases.] ongoing research,unassigned 3,0 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13460085&form=6&db=m [Activation of phosphoglucomutase in blood of hepatitis patients.] causal interaction,diagnostic usage,ongoing research,therapeutic application 4,2,2,1 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13639264&form=6&db=m Serum enzymes (transaminases, phosphoglucomutase, fumarase) in viral hepatitis during prednisone. (delta 1-cortisone) therapy. causal interaction,unassigned 1,0 5.4.2.2 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14026023&form=6&db=m [Phosphoglucomutase and hexokinase activities of various organs (liver, brain, kidney, myocardium) in the course of experimental MHV-3 hepatitis virus.] ongoing research,unassigned 1,0 5.4.2.2 Hepatitis, Viral, Human http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13451339&form=6&db=m [Phosphoglucomutase activity of blood in human viral hepatitis and in other icterogenic liver diseases.] ongoing research,unassigned 3,0 5.4.2.2 Hepatomegaly http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=822772&form=6&db=m Associations between polymorphic variety and disease susceptibility in two New Guinea populations. causal interaction,unassigned 2,0 5.4.2.2 Hypersensitivity http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15585009&form=6&db=m Identification of allergens responsible for canine cutaneous adverse food reactions to lamb, beef and cow's milk. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Hypersensitivity http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Hyperthyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1258096&form=6&db=m [Intraerythrocytic enzyme activities in euthyroid subjects and hyperthyroid patients before treatment and following stabilization of metabolism using radioiodine therapy] diagnostic usage,unassigned 1,0 5.4.2.2 Hypothyroidism http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26303607&form=6&db=m News on Clinical Details and Treatment in PGM1-CDG. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13793003&form=6&db=m [Metabolic aspects of hepatic tissue in infection of the mouse from EDP virus. I. Phosphoglucomutase, aldolase and enolase activity.] ongoing research,unassigned 4,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17170466&form=6&db=m A defect in carbohydrate metabolism ameliorates symptom severity in virus-infected Arabidopsis thaliana. ongoing research,unassigned 1,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22492233&form=6&db=m Changes in the contents of metabolites and enzyme activities in rice plants responding to Rhizoctonia solani Kuhn infection: activation of glycolysis and connection to phenylpropanoid pathway. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23173442&form=6&db=m [Effects of Brucella phosphoglucomutase on inducing infection of trophoblastic cells]. unassigned - 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26482871&form=6&db=m Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 (PGM3) gene. causal interaction,unassigned 2,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28536292&form=6&db=m Capsule Production and Glucose Metabolism Dictate Fitness during Serratia marcescens Bacteremia. therapeutic application,unassigned 1,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29877008&form=6&db=m Recombinant phosphoglucomutase and CAMP factor as potential subunit vaccine antigens induced high protection against Streptococcus iniae infection in flounder (Paralichthys olivaceus). therapeutic application,unassigned 3,0 5.4.2.2 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33534079&form=6&db=m Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations. causal interaction,diagnostic usage,therapeutic application,unassigned 4,4,1,0 5.4.2.2 Infertility, Male http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27588462&form=6&db=m Plastidic phosphoglucomutase and ADP-glucose pyrophosphorylase mutants impair starch synthesis in rice pollen grains and cause male sterility. unassigned - 5.4.2.2 Intestinal Volvulus http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11016441&form=6&db=m Phosphoglucomutase and trehalase isoenzymes of Venezuelan simulium vectors of Onchocerca volvulus. ongoing research,unassigned 1,0 5.4.2.2 Job Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25365149&form=6&db=m Hyper-IgE syndromes: reviewing PGM3 deficiency. causal interaction,unassigned 4,0 5.4.2.2 Job Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Job Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28702026&form=6&db=m Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population. causal interaction,unassigned 2,0 5.4.2.2 Leishmaniasis, Cutaneous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9574789&form=6&db=m Isoenzyme characterization of Leishmania isolated from human cases with localized cutaneous leishmaniasis from the State of Campeche, Yucatan Peninsula, Mexico. causal interaction,diagnostic usage,unassigned 1,1,0 5.4.2.2 Leishmaniasis, Cutaneous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24086789&form=6&db=m Development of Assays Using Hexokinase and Phosphoglucomutase Gene Sequences That Distinguish Strains of Leishmania tropica from Different Zymodemes and Microsatellite Clusters and Their Application to Palestinian Foci of Cutaneous Leishmaniasis. ongoing research,therapeutic application,unassigned 3,1,0 5.4.2.2 Leprosy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=162080&form=6&db=m Genetic markers and leprosy in South African negroes: Part II. Erythrocyte enzyme polymorphisms. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,1,0 5.4.2.2 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3160990&form=6&db=m Cytotoxic action of low dose Ara-C. Investigations in a marrow grafted patient with relapse. diagnostic usage,unassigned 1,0 5.4.2.2 Liver Abscess, Amebic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23514636&form=6&db=m Evaluation of Entamoeba histolytica recombinant phosphoglucomutase protein for serodiagnosis of amoebic liver abscess. therapeutic application,unassigned 2,0 5.4.2.2 Liver Cirrhosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6452554&form=6&db=m [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)] causal interaction,unassigned 4,0 5.4.2.2 Liver Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13451339&form=6&db=m [Phosphoglucomutase activity of blood in human viral hepatitis and in other icterogenic liver diseases.] ongoing research,unassigned 3,0 5.4.2.2 Loeys-Dietz Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Malaria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2936261&form=6&db=m Resistance to falciparum malaria among adults in central Sudan. causal interaction,therapeutic application,unassigned 2,1,0 5.4.2.2 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32057119&form=6&db=m A missense variant remote from the active site impairs stability of human phosphoglucomutase 1. causal interaction,unassigned 4,0 5.4.2.2 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23780368&form=6&db=m Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency. causal interaction,unassigned 4,0 5.4.2.2 Muscular Dystrophies http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14400396&form=6&db=m Phosphoglucomutase activity in hereditary muscular dystrophy in mice. ongoing research,unassigned 4,0 5.4.2.2 Muscular Dystrophy, Duchenne http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2931091&form=6&db=m Erythrocyte enzyme allotypes in the X-linked recessive disorders, Duchenne muscular dystrophy and haemophilia-A hemizygotes and heterozygotes. causal interaction,ongoing research,unassigned 1,1,0 5.4.2.2 Myocardial Infarction http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13811631&form=6&db=m [Transaminase and phosphoglucomutase activity of the blood of the coronary venous sinus after experimental myocardial infarct.] ongoing research,therapeutic application,unassigned 2,2,0 5.4.2.2 Myocardial Infarction http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22785563&form=6&db=m Phosphoglucomutase activity as a novel biomarker in patients with acute myocardial infarction. causal interaction,diagnostic usage,ongoing research,therapeutic application 4,4,3,2 5.4.2.2 Neoplasm Metastasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=404764&form=6&db=m [Geycogen content and the enzymatic system of its biosynthesis in normal and tumorous human tissues] ongoing research,unassigned 2,0 5.4.2.2 Neoplasm Metastasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31582909&form=6&db=m PGM5 is a promising biomarker and may predict the prognosis of colorectal cancer patients. causal interaction,unassigned 4,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=404764&form=6&db=m [Geycogen content and the enzymatic system of its biosynthesis in normal and tumorous human tissues] ongoing research,unassigned 2,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=508567&form=6&db=m Isoenzymes of hexokinase, 6-phosphogluconate dehydrogenase, phosphoglucomutase and lactate dehydrogenase in uterine cancer. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=667849&form=6&db=m A statistical model for predicting response of breast cancer patients to cytotoxic chemotherapy. diagnostic usage,ongoing research,unassigned 3,4,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=994214&form=6&db=m Human neoplastic and normal cells in tissue culture. I. Cell lines derived from malignant melanomas and normal melanocytes. diagnostic usage,ongoing research,unassigned 3,4,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2570483&form=6&db=m Characterization of a human follicular thyroid carcinoma cell line (UCLA RO 82 W-1). diagnostic usage,ongoing research,unassigned 3,4,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13811377&form=6&db=m [Observations on the behavior of erythrocytic phosphoglucomutase activity in patients with neoplasms and malignant blood diseases.] diagnostic usage,ongoing research,unassigned 3,2,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13939687&form=6&db=m [A study on serum phosphohexose-isomerase and serum phosphoglucomutase in the living body experimentally induced with cancer, with special reference to the relationship with operation.] diagnostic usage,ongoing research,unassigned 2,3,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14033929&form=6&db=m [A study on serum phosphohexose-isomerase and serum phosphoglucomutase in the living body experimentally induced with cancer, with special reference to the normal value and its locational differences of the cancers.] diagnostic usage,ongoing research,unassigned 2,3,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14209130&form=6&db=m [CLINICAL STUDIES ON SERUM GLYCOLYTIC ENZYMES IN CANCER PATIENTS; ON PHOSPHOHEXOSE ISOMERASE, PHOSPHOGLUCOMUTASE AND LACTIC DEHYDROGENASE ACTIVITIES.] diagnostic usage,ongoing research,unassigned 3,3,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17340808&form=6&db=m [Histochemical demonstration of glial enzyme activity. II. Reagent and neoplastic glia] causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30174305&form=6&db=m Fibroblasts Mobilize Tumor Cell Glycogen to Promote Proliferation and Metastasis. causal interaction,ongoing research,therapeutic application,unassigned 1,3,1,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31582909&form=6&db=m PGM5 is a promising biomarker and may predict the prognosis of colorectal cancer patients. causal interaction,unassigned 4,0 5.4.2.2 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32712171&form=6&db=m Kinetic modeling of glucose central metabolism in hepatocytes and hepatoma cells. unassigned - 5.4.2.2 Nephrosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13510477&form=6&db=m [Glycolytic activity in experimental nephrosis induced by anti-kidney serum. I. Aldolase; phosphoglucomutase.] unassigned - 5.4.2.2 Neutropenia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26409661&form=6&db=m Neonatal-onset T(-)B(-)NK(+) severe combined immunodeficiency and neutropenia caused by mutated phosphoglucomutase 3. unassigned - 5.4.2.2 Onchocerciasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2980977&form=6&db=m Population relationships of Simulium yahense and Simulium sanctipauli in the Firestone Rubber Plantation at Harbel, Liberia. unassigned - 5.4.2.2 Onchocerciasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11016441&form=6&db=m Phosphoglucomutase and trehalase isoenzymes of Venezuelan simulium vectors of Onchocerca volvulus. ongoing research,unassigned 1,0 5.4.2.2 Osteosarcoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1478667&form=6&db=m Syntenic conservation of HSP70 genes in cattle and humans. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1074344&form=6&db=m Acquired erythroenzymopathies in blood disorders: study of 200 cases. diagnostic usage,therapeutic application,unassigned 1,1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1385770&form=6&db=m [A case of adult onset phosphoglucomutase deficiency] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2791407&form=6&db=m [Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2942157&form=6&db=m [A case of phosphoglucomutase deficiency with decreased muscle and serum carnitine] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2965317&form=6&db=m Infantile muscle glycogen storage disease: phosphoglucomutase deficiency with decreased muscle and serum carnitine levels. causal interaction,diagnostic usage,unassigned 4,1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6452554&form=6&db=m [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9589990&form=6&db=m [Phosphoglucomutase deficiency] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11596382&form=6&db=m [Phosphoglucomutase deficiency] causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17259620&form=6&db=m Effects of alpha-phosphoglucomutase deficiency on cell wall properties and fitness in Streptococcus gordonii. ongoing research,unassigned 1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19625727&form=6&db=m Muscle glycogenosis due to phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24499211&form=6&db=m Multiple phenotypes in phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24849093&form=6&db=m Multiple phenotypes in phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24849094&form=6&db=m Multiple phenotypes in phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24972800&form=6&db=m Search for rare liver diseases: The case of glycosylation defects mimicking Wilson Disease ->. causal interaction,diagnostic usage,unassigned 1,1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25168163&form=6&db=m Mutations in hereditary phosphoglucomutase 1 deficiency map to key regions of enzyme structure and function. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25288802&form=6&db=m Compromised catalysis and potential folding defects in in vitro studies of missense mutants associated with hereditary phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26303607&form=6&db=m News on Clinical Details and Treatment in PGM1-CDG. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26972339&form=6&db=m Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 Deficiency. causal interaction,unassigned 4,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27663060&form=6&db=m What have we learned about glycogenosis in recent years? unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28794993&form=6&db=m Limitations of galactose therapy in phosphoglucomutase 1 deficiency. causal interaction,therapeutic application,unassigned 3,1,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28882528&form=6&db=m Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31956197&form=6&db=m [Electrophysiological evidence of impaired neuromuscular junction in a case of phosphoglucomutase 1 deficiency manifesting fluctuating muscle weakness]. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32101853&form=6&db=m [Erratum: [Advance Publication] Electrophysiological evidence of impaired neuromuscular junction in a case of phosphoglucomutase 1 deficiency manifesting fluctuating muscle weakness]. unassigned - 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32681750&form=6&db=m International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): Diagnosis, follow-up, and management. causal interaction,diagnostic usage,unassigned 4,2,0 5.4.2.2 phosphoglucomutase (alpha-d-glucose-1,6-bisphosphate-dependent) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33342467&form=6&db=m Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots. causal interaction,unassigned 2,0 5.4.2.2 phosphoglycerate kinase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2791407&form=6&db=m [Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies] causal interaction,unassigned 4,0 5.4.2.2 Precancerous Conditions http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21562899&form=6&db=m A signature of six genes highlights defects on cell growth and specific metabolic pathways in murine and human hepatocellular carcinoma. unassigned - 5.4.2.2 Precursor Cell Lymphoblastic Leukemia-Lymphoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2973848&form=6&db=m Subtyping of erythrocyte phosphoglucomutase-1 as a genetic marker for bone-marrow engraftment and hematopoietic chimerism after allogeneic bone-marrow transplantation in a patient with acute lymphoblastic leukemia. unassigned - 5.4.2.2 Primary Immunodeficiency Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30005381&form=6&db=m Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platform. diagnostic usage,therapeutic application,unassigned 2,3,0 5.4.2.2 Prostatic Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21159204&form=6&db=m Down-regulation of phosphoglucomutase 3 mediates sulforaphane-induced cell death in LNCaP prostate cancer cells. causal interaction,ongoing research,unassigned 2,2,0 5.4.2.2 Proteinuria http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=822772&form=6&db=m Associations between polymorphic variety and disease susceptibility in two New Guinea populations. causal interaction,unassigned 2,0 5.4.2.2 Rhabdomyolysis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24972800&form=6&db=m Search for rare liver diseases: The case of glycosylation defects mimicking Wilson Disease ->. causal interaction,diagnostic usage,unassigned 1,1,0 5.4.2.2 Sarcoma 180 http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2934389&form=6&db=m 5-Iodoribose 1-phosphate, an analog of ribose 1-phosphate. Enzymatic synthesis and kinetic studies with enzymes of purine, pyrimidine, and sugar phosphate metabolism. ongoing research,unassigned 3,0 5.4.2.2 Seizures http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=698019&form=6&db=m [Changes in cerebral glycogen content during strychnine convulsions. I. Behavior of phosphorylase and phosphoglucomutase with progressively increasing doses of the drug] causal interaction,therapeutic application,unassigned 2,1,0 5.4.2.2 Severe Combined Immunodeficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Severe Combined Immunodeficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26409661&form=6&db=m Neonatal-onset T(-)B(-)NK(+) severe combined immunodeficiency and neutropenia caused by mutated phosphoglucomutase 3. unassigned - 5.4.2.2 Severe Combined Immunodeficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29943473&form=6&db=m Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran. causal interaction,diagnostic usage,unassigned 4,4,0 5.4.2.2 Severe Combined Immunodeficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33534079&form=6&db=m Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations. causal interaction,diagnostic usage,therapeutic application,unassigned 4,4,1,0 5.4.2.2 Silicosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9662990&form=6&db=m [Genetic aspects of silicosis: polymorphic gene distribution frequency] diagnostic usage,ongoing research,unassigned 1,3,0 5.4.2.2 Silicosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12096683&form=6&db=m Genetic-biochemical criteria for individual sensitivity in development of occupational bronchopulmonary diseases. unassigned - 5.4.2.2 Skin Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=885537&form=6&db=m Psoriasis vulgaris and genetic markers. causal interaction,unassigned 1,0 5.4.2.2 Starvation http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=164319&form=6&db=m Effect of starvation on fructose diphosphatase, glucose-6-phosphatase and phosphoglucomutase activities in organs of Pseudemys (Chrysemys) scripta elegans. unassigned - 5.4.2.2 Stomach Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1210137&form=6&db=m [Serum phosphoglucomutase activity in stomach cancer patients] diagnostic usage,unassigned 4,0 5.4.2.2 Teratoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6961419&form=6&db=m Diverse origins of multiple ovarian teratomas in a single individual. diagnostic usage,unassigned 1,0 5.4.2.2 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6224013&form=6&db=m Association between phosphoglucomutase (PGM1) and group-specific component (Gc) subtypes and tuberculosis. causal interaction,unassigned 1,0 5.4.2.2 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22809717&form=6&db=m Heterologous expression and biochemical characterization of recombinant alpha phosphoglucomutase from Mycobacterium tuberculosis H37Rv. ongoing research,unassigned 4,0 5.4.2.2 Tuberous Sclerosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=166911&form=6&db=m Serum and tissue proteins in tuberous sclerosis. I. Serum and red-cell polymorphic systems. unassigned - 5.4.2.2 Uterine Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=508567&form=6&db=m Isoenzymes of hexokinase, 6-phosphogluconate dehydrogenase, phosphoglucomutase and lactate dehydrogenase in uterine cancer. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 5.4.2.2 Vitiligo http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6950922&form=6&db=m Distribution of serum proteins, red cell enzymes and haemoglobins in vitiligo. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,4,0 5.4.2.2 Wasting Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0 5.4.2.2 Wiskott-Aldrich Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26209898&form=6&db=m Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation. causal interaction,unassigned 3,0