IOGA (International Organization Of Glutaric Acidemia Bringing Information about the organization, their services and about the disease. Including events, newsletter, FAQs, message board and links. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: ExPASy Home page Site Map Search ExPASy Contact us Swiss-Prot Search Swiss-Prot/TrEMBL Swiss-Prot/TrEMBL (full text) PROSITE SWISS-2DPAGE ENZYME NEWT Taxonomy HAMAP families ExPASy web site for The ExPASy Server requires Javascript to be fully functional. You may not see all the information available for this page (More information) Entry info Name and origin References Comments ... Tools Note: most headings are clickable, even if they don't appear as links. They link to the user manual or other documents Entry information Entry name Primary accession number Secondary accession number Entered in Swiss-Prot in Release 30, October 1994 Sequence was last modified in Release 30, October 1994 Annotations were last modified in Release 48, September 2005 Name and origin of the protein Protein name Electron transfer flavoprotein beta-subunit Synonym Beta-ETF Gene name Name: ETFB From Homo sapiens (Human) TaxID Taxonomy ... References
Cardiac + Myopathy; Cardiomyopathy glutaricaciduria IIA) l Electron transfer flavoprotein, ? polypeptide ; Chromosome 15q23q25; Recessive http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Glutaricaciduria I glutaricaciduria I (GAI) is a rare hereditary metabolic disorder, caused by adeficiency of the enzyme glutaryl-CoA dehydrogenase. http://www.bchealthguide.org/kbase/nord/nord383.htm
Extractions: It is possible that the main title of the report Glutaricaciduria I is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Glutaricaciduria I (GA-I) is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of disorders known as "organic acidemias," it is characterized by an enlarged head (macrocephaly), decreased muscle tone (hypotonia), vomiting, and excess acid in the blood. Affected individuals may also have involuntary movements of the trunk and limbs (dystonia or athetosis) and mental retardation may also occur.
Glutaric Aciduria Type 1 Home Page Information and links for children with GA1. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Glutaricaciduria II glutaricaciduria II is one of the conditions termed organic acidemias. Individualswith these conditions have a deficiency or absence of an enzyme that http://www.bchealthguide.org/kbase/nord/nord378.htm
Extractions: It is possible that the main title of the report Glutaricaciduria II is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Glutaricaciduria II is one of the conditions termed organic acidemias. Individuals with these conditions have a deficiency or absence of an enzyme that prevents them from breaking down certain chenicals in the body, resulting the accumulation of several organic acids in the blood and urine. Two enzymes that may be deficient in glutaricaciduria II are electron transfer flavoprotein (ETF) and ETF-ubiquinone oxidoreductase (ETF:QO). A complete enzyme deficiency causes a severe form of the disorder termed neonatal glutaricaciduria ll that is associated with a short life span and, sometimes, with specific physical birth defects. The less severe form of the disorder is termed late onset glutaricaciduria ll and has an extremely variable age of onset. Symptoms include nausea, vomiting, weakness and low blood sugar (hypoglycemia). Glutaricaciduria II is inherited as an autosomal recessive genetic disorder.
Glutaricaciduria I glutaricaciduria I (GA I) is a rare hereditary metabolic disorder, caused bya deficiency of the enzyme http://my.webmd.com/hw/raising_a_family/nord383.asp
Extractions: Glutaricaciduria I (GA-I) is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of disorders known as "organic acidemias," it is characterized by an enlarged head (macrocephaly), decreased muscle tone (hypotonia), vomiting, and excess acid in the blood. Affected individuals may also have involuntary movements of the trunk and limbs (dystonia or athetosis) and mental retardation may also occur.
Glutaricaciduria II glutaricaciduria II is one of the conditions termed organic acidemias. Individualswith these conditions http://my.webmd.com/hw/raising_a_family/nord378.asp
Extractions: Glutaricaciduria II is one of the conditions termed organic acidemias. Individuals with these conditions have a deficiency or absence of an enzyme that prevents them from breaking down certain chenicals in the body, resulting the accumulation of several organic acids in the blood and urine. Two enzymes that may be deficient in glutaricaciduria II are electron transfer flavoprotein (ETF) and ETF-ubiquinone oxidoreductase (ETF:QO). A complete enzyme deficiency causes a severe form of the disorder termed neonatal glutaricaciduria ll that is associated with a short life span and, sometimes, with specific physical birth defects. The less severe form of the disorder is termed late onset glutaricaciduria ll and has an extremely variable age of onset. Symptoms include nausea, vomiting, weakness and low blood sugar (hypoglycemia). Glutaricaciduria II is inherited as an autosomal recessive genetic disorder.
Genetic Disorders / Glutaricaciduria Paloweb health conditions and diseases conditions genetic disorders glutaricaciduria http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
TerritorioScuola OpenDirectoryProject Health Conditions And Le risorse per la scuola, la formazione, l'universita' gli insegnanti, gli educatori. Educational resources on internet for teachers and learners. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Definitions Of Genetic Disorders-G glutaricaciduria II ga2.htm glutaricaciduria Type IIA ga2.htm glutaricaciduriaType IIB ga2.htm GlutarylCoA Dehydrogenase Deficiency ga1.htm http://www.icomm.ca/geneinfo/def-g.htm
Glutaricaciduria I glutaricaciduria I (GAI) is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
NORD - National Organization For Rare Disorders, Inc. glutaricaciduria II is one of the conditions termed organic acidemias. Two enzymes that may be deficient in glutaricaciduria II are electron transfer http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Glutaricacidu
