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hyperlysinemia - increased aminoacid lysine in blood Definition for hyperlysinemia Hyperlysinemia is a hereditary condition characterized by an abnormal increase of lysine in the blood and appears to be benign. It can be associated with saccharopine dehydrogenase. some common symptoms eye lens problems some related diagnoses 1 - 1 of 1 diagnoses homocystinuria   more do i have 'hyperlysinemia'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'hyperlysinemia' 1 - 5 of 9 diagnostic tests Plasma amino acids hyperlysinemia and Plasma amino acids urine amino acids hyperlysinemia and urine amino acids vision tests hyperlysinemia and vision tests α-aminoadipic semialdehyde synthase in cultured skin fibroblasts hyperlysinemia and α-aminoadipic semialdehyde synthase in cultured skin fibroblasts EEG - Electroencephalogram hyperlysinemia and EEG - Electroencephalogram serum lysine hyperlysinemia and serum lysine Molecular Genetic Studies hyperlysinemia and Molecular Genetic Studies Comprehensive eye exam hyperlysinemia and Comprehensive eye exam cultured skin fibroblasts for biochemical study hyperlysinemia and cultured skin fibroblasts for biochemical study for more please login, login is free (click to login) therapeutic procedures for 'hyperlysinemia'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for hyperlysinemia: therapeutic procedure search results for 'hyperlysinemia' rankings are computer generated. please consult your health care provider. medications search results for 'hyperlysinemia' rankings are computer generated. please consult your health care provider. web search results for hyperlysinemia Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - hyperlysinemia Hyperlysinemia - Wikipedia, the free encyclopedia ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... Retrieved from "http://en.wikipedia.org/wiki/Hyperlysinemia" ... http://en.wikipedia.org/wiki/Hyperlysinemia   en.wikipedia.org - summary Hyperlysinemia with saccharopinuria due to combined lysine ... Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate ... detailed investigation revealed hyperlysinemia and hyperlysinuria, with lesser ... http://www.ncbi.nlm.nih.gov/pubmed/571908   www.ncbi.nlm.nih.gov - summary Propionic acidemia and hyperlysinemia in a case with ornithine ... Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase ... hyperlysinemia and an unusual elevation of short chain fatty acids, mainly ... http://www.ncbi.nlm.nih.gov/pubmed/977722   www.ncbi.nlm.nih.gov - summary AASS - NextBio null: This gene encodes a bifunctional enzyme that catalyzes the first two steps ... Hyperlysinemia. Bhlhb8 gene. Pluripotent stem cell. Saccharopinuria. C38D4.6 gene ... http://www.nextbio.com/b/home/home.nb?id=38452&type=feature   www.nextbio.com - summary Morning Rounds: The Case of the Patient Who Had Cat Eyes Morning Rounds: The Case of the Patient Who Had Cat Eyes Eyenet, Donald M. ... Marfan's syndrome, homocystinuria, hyperlysinemia, aniridia, iris coloboma, ... http://www.aao.org/publications/eyenet/200504/am_rounds.cfm   www.aao.org - summary Identification of the alpha-aminoadipic semialdehyde synthase gene ... ... condition characterized by hyperlysinemia, lysinuria, and variable ... We sequenced the genomic DNA from a single patient with hyperlysinemia (JJa) ... http://www.ncbi.nlm.nih.gov/pubmed/10775527   www.ncbi.nlm.nih.gov - summary PMID 6434529 Hyperlysinemia type I is associated with a combined deficiency in lysine ... In familial hyperlysinemia type II, only saccharopine dehydrogenase activity is ... http://www.ncbi.nlm.nih.gov/pubmed/6434529   www.ncbi.nlm.nih.gov - summary Talk:Hyperlysinemia - Wikipedia, the free encyclopedia Talk:Hyperlysinemia. From Wikipedia, the free encyclopedia. Jump to: navigation, search ... Retrieved from "http://en.wikipedia.org/wiki/Talk:Hyperlysinemia" ... http://en.wikipedia.org/wiki/Talk:Hyperlysinemia   en.wikipedia.org - summary Inborn errors of amino acid metabolism Inborn errors of amino acid metabolism Disease Enzyme deficiency Symptoms ... thin blond hair Hyperlysinemia a -Aminoadipic semialdehyde dehydrogenase ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?db=Books&rid=stryer.table.3260   www.ncbi.nlm.nih.gov - summary 238700 http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238700   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Octobre ... Hits Mots-clés -586 1.23% orphanet 115 0.24% adrenoleucodistrofia 102 0.21 ... fitosterolemia.html 3 0.01% hydatidosis 3 0.01% hygrome 3 0.01% hyperlysinemia ... http://orphanet.orpha.net/stat/orphanet/search_200710.html   orphanet.orpha.net - summary Orphanet: Hyperlysinemia The portal for rare diseases and orphan drugs ... Hyperlysinemia. Orpha number. ORPHA2203. Prevalence of rare diseases. Unknown. Inheritance ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=2203   www.orpha.net - summary AceView: Gene:AASS, a comprehensive annotation of human, mouse and worm ... AceView offers a comprehensive annotation of human, mouse and nematode genes ... Mutations in this gene are associated with familial hyperlysinemia. ... http://www.ncbi.nlm.nih.gov/IEB/Research/Acembly/av.cgi?db=human&c=Gene&l=AASS   www.ncbi.nlm.nih.gov - summary Separation of ornithine and lysine activities of the ornithine ... Several lines of evidence are presented that an entity is present in ... in the HHH-syndrome, saccharopinuria, citrullinemia and hyperlysinemia. ... http://www.ncbi.nlm.nih.gov/pubmed/6409607   www.ncbi.nlm.nih.gov - summary AASS - Wikipedia, the free encyclopedia This article is an orphan, as few or no other articles link to it. ... semialdehyde synthase gene, which is defective in familial hyperlysinemia.". Am. J. Hum. ... http://en.wikipedia.org/wiki/AASS   en.wikipedia.org - summary MIM Gene map The OMIM Gene map presents the cytogenetic map location of disease genes and ... Hyperlysinemia, 238700 (3); Saccharopinuria, 268700 (1) R. 7q31.3. ANKRD7 ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l601047   www.ncbi.nlm.nih.gov - summary MIM Gene map The OMIM Gene map presents the cytogenetic map location of disease genes and ... Hyperlysinemia, 238700 (3); Saccharopinuria, 268700 (1) R ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l605317   www.ncbi.nlm.nih.gov - summary Saccharopinuria - Wikipedia, the free encyclopedia ... hyperlysinemia caused by a partial deficiency of the enzyme saccharopine ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Saccharopinuria   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mai 2006 ... Période du résumé: Mai 2006 - Mots-clés. Généré le 02-Jun-2006 23:18 MEST. Hits Mots-clés -660 1.26% adrenoleucodistrofia 464 0.88% orphanet 449 0.86 ... http://orphanet.orpha.net/stat/orphanet/search_200605.html   orphanet.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Septembre ... Période du résumé: Septembre 2006 - Mots-clés. Généré le 02-Oct-2006 22:10 MEST. Hits Mots-clés -519 1.10% adrenoleucodistrofia 406 0.86% orphanet 346 0.74 ... http://www.orpha.net/stat/orphanet/search_200609.html   www.orpha.net - summary Weill-Marchesani Syndrome -- GeneReviews -- NCBI Bookshelf GeneReviews provides information about selected national organizations and ... Hyperlysinemia is a rare metabolic disorder found to be caused by mutation in ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=weill-ms   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mars 2007 ... Période du résumé: Mars 2007 - Mots-clés. Généré le 01-Apr-2007 22:46 CEST. Hits Mots-clés -1188 1.57% ectrodactilia 580 0.76% adrenoleucodistrofia 473 0.62 ... http://orphanet.orpha.net/stat/orphanet/search_200703.html   orphanet.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Avril 2007 ... Période du résumé: Avril 2007 - Mots-clés. Généré le 01-May-2007 22:53 CEST. Hits Mots-clés -782 1.04% adrenoleucodistrofia 516 0.69% orphanet 255 0.34 ... http://www.orpha.net/stat/orphanet/search_200704.html   www.orpha.net - summary Argininosuccinic aciduria - Wikipedia, the free encyclopedia Argininosuccinic aciduria, also called argininosuccinic acidemia, is an ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Argininosuccinic_aciduria   en.wikipedia.org - summary Lysine Biosynthesis - NextBio Genes involved in lysine biosynthesis Source KEGG. ... Hyperlysinemia. Neurokinin B. Glomerulus. Pancreas Cancer. CCL19 gene. Reticulocyte ... http://www.nextbio.com/b/home/home.nb?id=199503&type=biogroup   www.nextbio.com - summary Ectopia lentis - Wikipedia, the free encyclopedia Ectopia lentis is a displacement or malposition of the eye's ... Hyperlysinemia. Less common: Ehlers-Danlos syndrome. Crouzon disease. Refsum syndrome ... http://en.wikipedia.org/wiki/Ectopia_lentis   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... Période du résumé: Juillet 2007 - Mots-clés. Généré le 01-Aug-2007 22:58 CEST. Hits Mots-clés -389 0.32% orphanet 353 0.29% vitiligo 248 0.21% lupus 239 0.20 ... http://orphanet.orpha.net/stat/orphanet/search_200707.html   orphanet.orpha.net - summary Histidinemia - Wikipedia, the free encyclopedia Histidinemia, also referred to as histidinuria, is a rare autosomal recessive ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Histidinemia   en.wikipedia.org - summary AASS - NextBio AASS: This gene encodes a bifunctional enzyme that catalyzes the first two steps ... Hyperlysinemia. Bhlhb8 gene. Pluripotent stem cell. Saccharopinuria. C38D4.6 gene ... http://www.nextbio.com/b/home/home.nb?q=AASS&id=38452&name=AASS&type=GENE   www.nextbio.com - summary MERCK MANUALS Disorders of phenylalanine and tyrosine metabolism. Phenylketonuria (PKU; classic and mild forms; ... Hyperlysinemia (238700) Lysine: ?-ketoglutarate ... http://www.merck.com/media/mmpe/pdf/Table_296-1w.pdf   www.merck.com - summary Homocystinuria - Wikipedia, the free encyclopedia This article does not cite any references or sources. ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Homocystinuria   en.wikipedia.org - summary Hyperammonemia - Wikipedia, the free encyclopedia neuro/162 ped/1057. MeSH. D022124. Hyperammonemia (or 'hyperammonaemia' ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Hyperammonemia   en.wikipedia.org - summary Allysine(L-allysine) - NextBio ... hemoglobin hydrosulfide hypercapnia hyperlysinemia IGKV1D-39 l-allysine liver ... semialdehyde synthase gene, which is defective in familial hyperlysinemia. ... http://www.nextbio.com/b/home/home.nb?q=L-allysine&id=39151&...   www.nextbio.com - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Decembre ... Hits Mots-clés -406 2.08% orphanet 117 0.60% orpha 86 0.44% syndrome de ... polyclonale 2 0.01% hyperlysinemia 2 0.01% hypermobility more. ... http://www.orpha.net/stat/orphanet/search_200712.html   www.orpha.net - summary Ochronosis - Wikipedia, the free encyclopedia This article needs additional citations for verification. ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Ochronosis   en.wikipedia.org - summary OMIM Update List for August, 2000 113995 COMPLEMENT COMPONENT 5 RECEPTOR 1; C5R1. 116806 CATENIN, BETA-1; CTNNB1. 118455 CYTOCHROME P450, ... 238700 HYPERLYSINEMIA. 268700 SACCHAROPINURIA ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.2000   www.ncbi.nlm.nih.gov - summary SJ Gould - NextBio You must enable JavaScript to run the NextBio application. author SJ Gould ... hyperlysinemia isoform L-Pipecolic acid Lipid rafts long-chain acyl-CoAs malonyl ... http://www.nextbio.com/b/literature/literature.nb?author=SJ+Gould   www.nextbio.com - summary Organic acidemia - Wikipedia, the free encyclopedia The four main types of organic acidemia are: methylmalonic acidemia, propionic ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Organic_acidemia   en.wikipedia.org - summary PubMed Link Image ... Apr Pediatrics A case of hyperlysinemia: biochemical and clinical observations. 546-54 Armstrong M D MD Robinow M M eng Case Reports Journal Article UNITED ... http://www.ncbi.nlm.nih.gov/pubmed/6022933   www.ncbi.nlm.nih.gov - summary Tetrahydrobiopterin deficiency - Wikipedia, the free encyclopedia Tetrahydrobiopterin deficiency (also known as BH4 deficiency) is a rare disorder ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Tetrahydrobiopterin_deficiency   en.wikipedia.org - summary Hyperkeratotic papil - Hypermelanosis due t You must enable JavaScript to run the NextBio application ... Hyperlysinemia, NOS. Hyperlysinemia, NOS (search) DISEASE. Hyperlysinuria with hyperammonaemia ... http://www.nextbio.com/b/sitemap/sitemap.nb?q=disease/a-z//h/H_4543-4603.nb   www.nextbio.com - summary 3-Methylcrotonyl-CoA carboxylase deficiency - Wikipedia, the free ... 3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency), also known as 3 ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/3-Methylcrotonyl-CoA_carboxylase_deficiency   en.wikipedia.org - summary Alkaptonuria - Wikipedia, the free encyclopedia Alkaptonuria (black urine disease or alcaptonuria) is a rare inherited genetic ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Alkaptonuria   en.wikipedia.org - summary MERCK MANUALS DISORDERS OF FATTY ACID, VERY LONG-CHAIN FATTY ACID, AND GLYCEROL METABOLISM. DISEASE ... Biochemical pro?le: Hyperlysinemia, low plasma carnitine, 2-trans,4-cis ... http://www.merck.com/media/mmpe/pdf/Table_296-3w.pdf   www.merck.com - summary Carbamoyl phosphate synthetase I deficiency - Wikipedia, the free ... Please help improve this article by adding reliable references (ideally, ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Carbamoyl_phosphate_synthetase_I_deficiency   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juin 2007 ... Période du résumé: Juin 2007 - Mots-clés. Généré le 01-Jul-2007 22:49 CEST. Hits Mots-clés -441 0.32% adrenoleucodistrofia 439 0.32% klinefelter 412 0.30 ... http://www.orpha.net/stat/orphanet/search_200706.html   www.orpha.net - summary Fanconi syndrome - Wikipedia, the free encyclopedia Fanconi Syndrome (also known as Fanconi's syndrome) is a disorder in which the ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Fanconi_syndrome   en.wikipedia.org - summary Fumarase deficiency - Wikipedia, the free encyclopedia Fumarase deficiency (or fumaric aciduria) is an autosomal recessive metabolic ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Fumarase_deficiency   en.wikipedia.org - summary Ocular albinism - Wikipedia, the free encyclopedia Ocular albinism is a form of albinism which, in contrast to oculocutaneous ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Ocular_albinism   en.wikipedia.org - summary Ornithine transcarbamylase deficiency - Wikipedia, the free encyclopedia Ornithine transcarbamylase deficiency (OTCD), the most common of the urea cycle ... acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic acidemia · Saccharopinuria ... http://en.wikipedia.org/wiki/Ornithine_transcarbamylase_deficiency   en.wikipedia.org - summary show more 1  2