1. UniProt Knowledgebase Keyword: Glutaricaciduria Protein which, if defective, causes glutaricaciduria (GA), SRS Query.libs={swiss_prot}keywords glutaricaciduria libs-keywords glutaricaciduria. http://www.expasy.org/cgi-bin/get-entries?KW=Glutaricaciduria

2. NORD - National Organization For Rare Disorders, Inc. Offers alternate names, a general discussion and resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Glutaricacidu

3. 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

4. UniProtKB/Swiss-Prot Entry P38117 [ETFB_HUMAN] Electron Transfer Flavoprotein Be DISEASE Defects in ETFB are the cause of glutaric aciduria typeIIB (GAIIB) MIM231680; also known as glutaricaciduria IIB. http://www.expasy.org/uniprot/P38117

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) UniProtKB/Swiss-Prot entry 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 NUCLEOTIDE SEQUENCE [MRNA]. TISSUE Fetal liver PubMed=8504797 [ NCBI ExPASy EBI Israel ... Didonato S. "cDNA cloning and mitochondrial import of the beta-subunit of the human electron-transfer flavoprotein."; Eur. J. Biochem. 213:1003-1008(1993).

5. 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

6. 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

var hwPrint=1;var hwDocHWID="nord383";var hwDocTitle="Glutaricaciduria I";var hwRank="1";var hwSectionHWID="nord383-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Glutaricaciduria I Important 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. Synonyms Dicarboxylic Aminoaciduria GA I Glutaric Acidemia I Glutaric Aciduria I Glutaricacidemia I Glutaryl-CoA Dehydrogenase Deficiency Glutaurate-Aspartate Transport Defect Disorder Subdivisions None General Discussion 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. Babies with glutaricaciduria I are sometimes mistakenly thought by medical professionals to be abused babies because they present with subdural and/or retinal hemorrhages.

7. 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

8. 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

var hwPrint=1;var hwDocHWID="nord378";var hwDocTitle="Glutaricaciduria II";var hwRank="1";var hwSectionHWID="nord378-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Glutaricaciduria II Important 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. Synonyms GA II Glutaric Acidemia II Glutaric Aciduria II Glutaricacidemia II Multiple Acyl-Co-A Dehydrogenation Deficiency MADD Electron Transfer Flavoprotein: Ubiquinone Oxidoreductase, Deficiency of Electron Transfer Flavoprotein, Deficiency of Disorder Subdivisions None General Discussion 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.

9. The Knowledge.com T Directory - Health - Conditions And Diseases - The knowledge.com glutaricaciduria directory with links and news. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. 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

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Glutaricaciduria I Important 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. Synonyms Dicarboxylic Aminoaciduria GA I Glutaric Acidemia I Glutaric Aciduria I Glutaricacidemia I Glutaryl-CoA Dehydrogenase Deficiency Glutaurate-Aspartate Transport Defect Disorder Subdivisions None General Discussion 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. Babies with glutaricaciduria I are sometimes mistakenly thought by medical professionals to be abused babies because they present with subdural and/or retinal hemorrhages.

11. Health Conditions And Diseases Genetic Disorders Glutaricaciduria Health, Conditions and Diseases, Genetic Disorders, glutaricaciduria can be found in the links section at Computer Rescue 911! http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. 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

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Glutaricaciduria II Important 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. Synonyms GA II Glutaric Acidemia II Glutaric Aciduria II Glutaricacidemia II Multiple Acyl-Co-A Dehydrogenation Deficiency MADD Electron Transfer Flavoprotein: Ubiquinone Oxidoreductase, Deficiency of Electron Transfer Flavoprotein, Deficiency of Disorder Subdivisions None General Discussion 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.

13. 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

14. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/ More news about glutaricaciduria . Error We did not find any matches for NORD glutaricaciduria I Offers alternate names, a general discussion and http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Genetic Disorders : Glutaricaciduria Subtopics See Also: Health: Conditions and Diseases: Nutrition and Metabolism Disorders Health: Conditions and Diseases: Rare Disorders Search Google: Glutaricaciduria News Books Links [ More news about Glutaricaciduria Error: We did not find any matches for your request. [ More books about Glutaricaciduria Glutaric Aciduria Type 1 - Information and links for children with GA1. IOGA: International Organization of Glutaric Acidemia - Information about the organization, their services and about the disease. Including events, newsletter, FAQs, message board and links. NORD: Glutaricaciduria I - Offers alternate names, a general discussion and resources. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Can't find it? Try searching Science Daily or the entire web with: Web sciencedaily.com

15. 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

16. Glutaricaciduria II,GA II,Glutaric Acidemia II,Glutaric Aciduria glutaricaciduria II,GA II,Glutaric Acidemia II,Glutaric Aciduria II GlutaricacidemiaII,glutaricaciduria Type IIA,GA IIA,Multiple AcylCoA Dehydrogenase http://www.icomm.ca/geneinfo/ga2.htm

17. S Gning.dk - Health Conditions And Diseases Genetic Disorders NORD glutaricaciduria I. Offers alternate names, a general discussion and resources. www.rarediseases.org http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. 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

19. 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

20. 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

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