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hereditary methemoglobinemia - condition caused by abnormally high levels of methemoglobin in blood Definition for hereditary methemoglobinemia Methemoglobinemia, also known as "met-Hb", is a disorder characterized by the presence of a higher than normal level of methemoglobin in the blood. more Methemoglobinemia, also known as "met-Hb", is a disorder characterized by the presence of a higher than normal level of methemoglobin in the blood. Methemoglobin is a form of hemoglobin that does not bind oxygen. When its concentration is elevated in red blood cells a functional anemia and tissue hypoxia may occur. less some common symptoms blue lips or dusky skin some related diagnoses 1 - 7 of 99 diagnoses congenital heart disease cystic fibrosis congenital abnormalities coronary arteries patent foramen ovale Pickwickian Syndrome hereditary hemorrhagic telangiectasia ciliary dyskinesia   more do i have 'hereditary methemoglobinemia'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'hereditary methemoglobinemia' 1 - 5 of 25 diagnostic tests Co-oximetry hereditary methemoglobinemia and Co-oximetry Hemoglobin electrophoresis hereditary methemoglobinemia and Hemoglobin electrophoresis methemoglobin reductase measurements hereditary methemoglobinemia and methemoglobin reductase measurements Arterial Blood Gas hereditary methemoglobinemia and Arterial Blood Gas Pulse oximetry Oximetry hereditary methemoglobinemia and Pulse oximetry Urinalysis Examination of urine to detect disease hereditary methemoglobinemia and Urinalysis Potassium cyanide test hereditary methemoglobinemia and Potassium cyanide test Molecular Genetic Studies hereditary methemoglobinemia and Molecular Genetic Studies filter paper bedside test hereditary methemoglobinemia and filter paper bedside test BUN hereditary methemoglobinemia and BUN Complete Blood Count hereditary methemoglobinemia and Complete Blood Count Complete metabolic panel hereditary methemoglobinemia and Complete metabolic panel G-6-PD screen hereditary methemoglobinemia and G-6-PD screen Lactate dehydrogenase (LDH) hereditary methemoglobinemia and Lactate dehydrogenase (LDH) Liver Function Tests elevated liver enzymes hereditary methemoglobinemia and Liver Function Tests Peripheral blood smear hereditary methemoglobinemia and Peripheral blood smear Reticulocyte count hereditary methemoglobinemia and Reticulocyte count Serum Creatinine hereditary methemoglobinemia and Serum Creatinine Serum haptoglobin hereditary methemoglobinemia and Serum haptoglobin Total bilirubin hereditary methemoglobinemia and Total bilirubin direct bilirubin hereditary methemoglobinemia and direct bilirubin Methemoglobin level hereditary methemoglobinemia and Methemoglobin level Methylene blue test hereditary methemoglobinemia and Methylene blue test serum electrolytes hereditary methemoglobinemia and serum electrolytes urine output hereditary methemoglobinemia and urine output for more please login, login is free (click to login) therapeutic procedures for 'hereditary methemoglobinemia'? 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 hereditary methemoglobinemia: therapeutic procedure search results for 'hereditary methemoglobinemia' 1 - 1 of 1 therapeutic procedures rankings are computer generated. please consult your health care provider. Intravenous (IV) glucose hereditary methemoglobinemia and Intravenous (IV) glucose medications search results for 'hereditary methemoglobinemia' 1 - 3 of 3 medications rankings are computer generated. please consult your health care provider.   methylene blue hereditary methemoglobinemia and methylene blue   ascorbic acid hereditary methemoglobinemia and ascorbic acid   riboflavin hereditary methemoglobinemia and riboflavin web search results for hereditary methemoglobinemia Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - hereditary methemoglobinemia Orphanet: Hereditary methemoglobinemia The portal for rare diseases ... Hereditary methemoglobinemia (HM) is a rare red cell ... congenital (or hereditary) methemoglobinemia types I and ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=621   www.orpha.net - summary Enzymatic instability of NADH-cytochrome b5 reductase as a cause of ... ... three independent probands of hereditary methemoglobinemia type I. Patients in ... deficiency to red cells in hereditary methemoglobinemia type I may be generally ... http://www.ncbi.nlm.nih.gov/pubmed/1400360   www.ncbi.nlm.nih.gov - summary Exonic point mutations in NADH-cytochrome B5 reductase genes of ... ... cytochrome b5 reductase gene of hereditary methemoglobinemia type I and type III, ... enzyme defects in hereditary methemoglobinemia are discussed. ... http://www.ncbi.nlm.nih.gov/pubmed/1707593   www.ncbi.nlm.nih.gov - summary Methemoglobinemia - Wikipedia, the free encyclopedia Methemoglobinemia is a disorder characterized by the presence of a higher than ... Hereditary: Fanconi anemia · Diamond-Blackfan anemia ... http://en.wikipedia.org/wiki/Methemoglobinemia   en.wikipedia.org - summary Serine-proline replacement at residue 127 of NADH-cytochrome b5 ... Hereditary methemoglobinemia is an autosomal recessive disorder characterized by ... for hereditary methemoglobinemia, generalized type, and compared its nucleotide ... http://www.ncbi.nlm.nih.gov/pubmed/2107882   www.ncbi.nlm.nih.gov - summary Blood/lymphatic system - Genetics Home Reference Anemia, hereditary sideroblastic see X-linked sideroblastic anemia ... blue baby syndrome see methemoglobinemia, beta-globin type ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/bloodlymphaticsystem   ghr.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Topics beginning with H-Hf Hemoglobin M disease see Methemoglobinemia. Hemoglobin SS disease (Hb SS) see Sickle cell anemia ... Hereditary fructose intolerance ... http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_H-Hf.htm   www.nlm.nih.gov - summary A novel point mutation in a 3' splice site of the NADH-cytochrome b5 ... Hereditary methemoglobinemia with generalized deficiency of NADH-cytochrome b5 ... to the phenotype of hereditary methemoglobinemia of the generalized type. ... http://www.ncbi.nlm.nih.gov/pubmed/7668255   www.ncbi.nlm.nih.gov - summary Rasburicase (Intravenous Route) - MayoClinic.com ... (G6PD) deficiency (a hereditary metabolic disorder affecting red ... Methemoglobinemia reactions (or history of)?Rasburicase should not be used if ... http://www.mayoclinic.com/health/drug-information/DR601505   www.mayoclinic.com - summary Hereditary elliptocytosis - Wikipedia, the free encyclopedia 3.1 Common hereditary elliptocytosis. 3.2 Spherocytic elliptocytosis ... Methemoglobinemia · Sulfhemoglobinemia. Coagulation/ coagulopathy/ bleeding diathesis ... http://en.wikipedia.org/wiki/Hereditary_elliptocytosis   en.wikipedia.org - summary An in-frame deletion of codon 298 of the NADH-cytochrome b5 reductase ... ... gene results in hereditary methemoglobinemia type II (generalized type) ... of a patient of type II hereditary methemoglobinemia found in Yokohama, Japan. ... http://www.ncbi.nlm.nih.gov/pubmed/8119939   www.ncbi.nlm.nih.gov - summary Chromosome 11 - Conditions related to genes on chromosome 11 - Genetics ... distal hereditary motor neuropathy, type V. enlarged parietal foramina ... methemoglobinemia, beta-globin type. multiple endocrine neoplasia ... http://ghr.nlm.nih.gov/chromosome=11/show/Conditions   ghr.nlm.nih.gov - summary Table of Contents: Medicine, Ob/Gyn, Psychiatry, and Surgery Methemoglobinemia. Monoclonal Gammopathies of Uncertain Origin. Mucosa ... Porphyria, Hereditary Coproporphyria. Protein C Deficiency. Protein S Deficiency ... http://author.emedicine.com/med/HEMATOLOGY.htm   author.emedicine.com - summary Hereditary persistence of fetal hemoglobin - Wikipedia, the free ... Hereditary persistence of foetal haemoglobin with beta-chain ... Methemoglobinemia · Sulfhemoglobinemia. Coagulation/ coagulopathy/ bleeding diathesis ... http://en.wikipedia.org/wiki/Hereditary_persistence_of_fetal_hemoglobin   en.wikipedia.org - summary 2008 MeSH Tree Structures. C15 - Hemic and Lymphatic Diseases Elliptocytosis, Hereditary [C15.378.071.141.150.365] ... Methemoglobinemia [C15.378.619] Pancytopenia [C15.378.700] Polycythemia [C15.378.738] ... http://www.nlm.nih.gov/mesh/trees2008/C15.html   www.nlm.nih.gov - summary Blood and Blood Disorders - Genetics Home Reference hereditary hemorrhagic telangiectasia. Job syndrome. McLeod ... methemoglobinemia, beta-globin type. neuroferritinopathy. paroxysmal nocturnal hemoglobinuria ... http://ghr.nlm.nih.gov/conditionGroup=bloodandblooddisorders   ghr.nlm.nih.gov - summary respiratory distress syndrome, hepatopulmonary syndrome, acute lung injury 104. Kurapati S, Mehta AC, Jain P. Benzocaine-induced methemoglobinemia. ... a patient with pulmonary hypertension and hereditary hemorrhagic telangiectasia. ... http://my.clevelandclinic.org/pulmonary/research_and_educati...   my.clevelandclinic.org - summary Recessive hereditary methaemoglobinaemia, type II: delineation of the ... Type II recessive hereditary methaemoglobinaemia (RHM) is a rare ... Methemoglobinemia/complications. Methemoglobinemia/diagnosis* Methemoglobinemia/genetics ... http://www.ncbi.nlm.nih.gov/pubmed/18202104   www.ncbi.nlm.nih.gov - summary Search Results - Genetics Home Reference In addition to the Genetics Home Reference results, you may be ... hereditary hemorrhagic telangiectasia ... methemoglobinemia, beta-globin type ... http://ghr.nlm.nih.gov/search?query="Lymphatic+Diseases"   ghr.nlm.nih.gov - summary Search Results - Genetics Home Reference Related classification: Hemic and Lymphatic Diseases. Related genes: MTTP ... hereditary hemorrhagic telangiectasia ... methemoglobinemia, beta-globin type ... http://ghr.nlm.nih.gov/search?query="Lymphatic+Diseases"&show=conditions   ghr.nlm.nih.gov - summary Prilocaine-Induced Methemoglobinemia -- Wisconsin, 1993 Methemoglobinemia is an uncommon disorder in which hemoglobin is not oxidized ... cardiovascular systems), persons with hereditary deficiencies of glucose-6 ... http://www.cdc.gov/mmwr/preview/mmwrhtml/00032499.htm   www.cdc.gov - summary Normal pulse oximeter reading in a cyanotic infant. ... presented with central cyanosis was found to have hereditary methaemoglobinaemia. ... Methemoglobinemia/blood. Methemoglobinemia/complications ... http://www.ncbi.nlm.nih.gov/pubmed/11168881   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Avril 2006 ... ... 9 0.02% agenesia del cuerpo calloso 9 0.02% albright hereditary osteodystrophy 9 ... 7 0.02% hemofilia 7 0.02% hereditary methemoglobinemia 7 0.02% hhh syndrome 7 ... http://www.orpha.net/stat/orphanet/search_200604.html   www.orpha.net - summary OMIM Update List for January, 2003 241530 HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY; HHRH ... 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?1.2003   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mai 2006 ... ... 12 0.02% glicogenose tipo ii 12 0.02% hereditary angioneurotic edema 12 ... 5 0.01% hepatoblastome 5 0.01% hereditary methemoglobinemia 5 0.01% hhh 5 0.01 ... http://www.orpha.net/stat/orphanet/search_200605.html   www.orpha.net - summary OMIM Update List for April, 2005 605285 NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE ... 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE. 306700 HEMOPHILIA A ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2005   www.ncbi.nlm.nih.gov - summary OMIM Update List for April, 2008 300704 PROSTATE CANCER, HEREDITARY, X-LINKED 2; HPCX2 ... LYMPHEDEMA, HEREDITARY, IB. 611969 ... 250790 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2008   www.ncbi.nlm.nih.gov - summary CYB5R3 - Wikipedia, the free encyclopedia ... b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type) ... gene results in hereditary methemoglobinemia type II (generalized type) ... http://en.wikipedia.org/wiki/CYB5R3   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Septembre ... ... pierre robin 14 0.03% adep 14 0.03% albright hereditary osteodystrophy ... fulminante 4 0.01% hereditary methemoglobinemia 4 0.01% herpetic encephalopathy ... http://www.orpha.net/stat/orphanet/search_200609.html   www.orpha.net - summary Alphabetical Index: Medicine, Ob/Gyn, Psychiatry, and Surgery Methemoglobinemia. Microscopic Polyangiitis. Microsporidiosis. Miliary Tuberculosis ... Spherocytosis, Hereditary. Spinal Cord Abscess ... http://author.emedicine.com/med/topiclist.htm   author.emedicine.com - summary OMIM Update List for June, 2001 122000 CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR ... 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?6.2001   www.ncbi.nlm.nih.gov - summary A Pekrun - NextBio Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon ... Hereditary methemoglobinemia due to reduced nicotin amide adenine dinucleotide ... http://www.nextbio.com/b/literature/literature.nb?author=A+Pekrun   www.nextbio.com - summary OMIM Update List for July, 1998 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... WITH HYPERCALCIURIA, HEREDITARY; HHRH ... 602089 HEMANGIOMA, HEREDITARY CAPILLARY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1998   www.ncbi.nlm.nih.gov - summary List of diseases (H) - Wikipedia, the free encyclopedia Heart hypertrophy, hereditary. Heart situs anomaly. Heart tumor ... Hereditary methemoglobinemia, recessive. Hereditary myopathy with intranuclear filamentous ... http://en.wikipedia.org/wiki/List_of_diseases_(H)   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Novembre ... ... hereditary methemoglobinemia 8 0.01% hidradenite 8 0.01% himenolepiasis 8 0.01 ... 4 0.01% albright's hereditary osteodystrophy 4 0.01% alcaptonÚria ... http://www.orpha.net/stat/orphanet/search_200611.html   www.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Decembre ... ... essencial 20 0.04% albright hereditary osteodystrophy 20 0.04% aromatase ... hemangiopericytoma 5 0.01% hemivertebras 5 0.01% hereditary methemoglobinemia 5 ... http://www.orpha.net/stat/orphanet/search_200612.html   www.orpha.net - summary www.nextbio.com/b/sitemap/sitemap.nb?q=disease/a-z//h/H_2352-2412.nb Hereditary liability to pressure palsies. Hereditary ... Hereditary methemoglobinemia, enzymatic type. Hereditary methemoglobinemia, enzymatic type (search) ... http://www.nextbio.com/b/sitemap/sitemap.nb?q=disease/a-z//h/H_2352-2412.nb   www.nextbio.com - summary OMIM Update List for December, 2002 122000 CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR ... Clinical Synopsis for 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.2002   www.ncbi.nlm.nih.gov - summary Cytochrome b5, type A - Wikipedia, the free encyclopedia Defects in CYB5A are the cause of type IV hereditary methemoglobinemia. [edit] References ... Congenital methemoglobinemia with a deficiency of cytochrome b5. ... http://en.wikipedia.org/wiki/Cytochrome_b5,_type_A   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juin 2007 ... ... de fallot 44 0.03% albright hereditary osteodystrophy 44 0.03% amiloidosis 44 ... 10 0.01% hereditary methemoglobinemia 10 0.01% hereditary persistence of ... http://www.orpha.net/stat/orphanet/search_200706.html   www.orpha.net - summary OMIM Update List for March, 2002 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... 605839 LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2002   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... ... syndrome sec 13 0.04% tirosinemia 13 0.04% x 12 0.04% hereditary angioneurotic ... oculocutaneo 3 0.01% albright's hereditary osteodystrophy 3 0.01% alfa 1 ... http://orphanet.orpha.net/stat/orphanet/search_200607.html   orphanet.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... ... hereditary osteodystrophy 51 0.04% aldolasa 51 0.04% displasia fibrosa 50 0.04 ... hemivertebras 7 0.01% hereditary methemoglobinemia 7 0.01% hermafroditismo ... http://www.orpha.net/stat/orphanet/search_200707.html   www.orpha.net - summary Terry Fugate-Wilcox - Wikipedia, the free encyclopedia This article may require cleanup to meet Wikipedia's quality standards. ... of Troublesome Creek, Kentucky, a family with hereditary methemoglobinemia. ... http://en.wikipedia.org/wiki/Terry_Fugate-Wilcox   en.wikipedia.org - summary OMIM Update List for March, 2004 158590 NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE II ... 187260 TELANGIECTASIA, HEREDITARY BENIGN ... 187900 THROMBASTHENIA-THROMBOCYTOPENIA, HEREDITARY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2004   www.ncbi.nlm.nih.gov - summary OMIM Update List for May, 2003 603528 DEHYDRATED HEREDITARY STOMATOCYTOSIS, PSEUDOHYPERKALEMIA, AND PERINATAL ... 250800 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?5.2003   www.ncbi.nlm.nih.gov - summary Table of Contents: Pediatrics Hemophilia A and B. Hemophilia C. Hereditary Disorders of Red Cell Permeability ... Methemoglobinemia. Myelodysplasia. Myelofibrosis. Osler-Weber-Rendu Syndrome ... http://author.emedicine.com/ped/HEMATOLOGY.htm   author.emedicine.com - summary OMIM Update List for June, 1998 176450 SACRAL AGENESIS, HEREDITARY, WITH PRESACRAL MASS, ANTERIOR MENINGOCELE, ... 250790 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?6.1998   www.ncbi.nlm.nih.gov - summary OMIM Update List for July, 1999 194380 DEHYDRATED HEREDITARY STOMATOCYTOSIS; DHS. 212070 CARBOXYPEPTIDASE N DEFICIENCY ... 250790 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5. 252500 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1999   www.ncbi.nlm.nih.gov - summary OMIM Update List for September, 1998 601518 PROSTATE CANCER, HEREDITARY 1 ... 132700 EPITHELIOMA, HEREDITARY MULTIPLE BENIGN CYSTIC ... 250790 METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?9.1998   www.ncbi.nlm.nih.gov - summary show more 1  2