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120 Possible Causes for Homocystinemia

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  • Homocystinuria without Methylmalonic Aciduria Type cblG

    Homocystinuria without methylmalonic aciduria is a rare metabolic disorder. There are three types of the disease, all of which are inherited in an autosomal recessive manner and caused by a functional deficiency of methionine synthase. Homocystinuria without methylmalonic aciduria type cblG is the result of[…][symptoma.com]

  • Homocystinuria without Methylmalonic Aciduria Type cblE

    Homocystinuria without methylmalonic aciduria is a rare metabolic disorder. There are three types of the disease, all of which are inherited in an autosomal recessive manner and caused by a functional deficiency of methionine synthase. Homocystinuria without methylmalonic aciduria type cblE is the result of[…][symptoma.com]

  • Homocystinuria

    Type 1 Excludes cystinosis ( E72.04 ) cystinuria ( E72.01 ) transcobalamin II deficiency ( D51.2 ) Disorders of sulfur-bearing amino-acid metabolism Approximate Synonyms Homocystinemia[icd10data.com] […] methylenetetrahydrofolate reductase Disorder of sulfur-bearing amino acid metabolism Disorder of sulphur bearing amino acid metabolism Heterozygous methylenetetrahydrofolate reductase mutation Homocystinemia[icd9data.com] Other Names Classic homocystinuria Homocystinemia Cystathionine beta-synthase deficiency (CBS) Disorder Category An amino acidemia Screening Finding Elevated methionine Tested[medicalhomeportal.org]

  • Disorder of Sulfur-Bearing Amino Acid Metabolism

    Methioninemia Homocystinemia, homocystinuria Hyperhomocysteinemia Hypermethioninemia Cystathionine synthase deficiency Cystathioninemia Cystathioninuria Disease, diseased[icd.codes] […] methylenetetrahydrofolate reductase Disorder of sulfur-bearing amino acid metabolism Disorder of sulphur bearing amino acid metabolism Heterozygous methylenetetrahydrofolate reductase mutation Homocystinemia[icd9data.com] Other Names Classic homocystinuria Homocystinemia Cystathionine beta-synthase deficiency (CBS) Disorder Category An amino acidemia Screening Finding Elevated methionine Tested[medicalhomeportal.org]

  • Cystathioninuria

    […] methylenetetrahydrofolate reductase Disorder of sulfur-bearing amino acid metabolism Disorder of sulphur bearing amino acid metabolism Heterozygous methylenetetrahydrofolate reductase mutation Homocystinemia[icd9data.com] […] hydroxycobalamin, methionine, betaine Methylmalonic acidemia-homocystinuria (cblE; 236270) Methionine synthase reductase MTRR (5p15)* Biochemical profile: Homocystinuria, homocystinemia[merckmanuals.com] […] supplementation Methylenetetrahydrofolate reductase deficiency (236250) Methylenetetrahydrofolate reductase MTHFR (1p36.3)* Biochemical profile: Low to normal plasma methionine, homocystinemia[merckmanuals.com]

  • Sagittal Sinus Thrombosis

    She presented elevated plasma levels of homocystinemia, a sulphur containing amino acid that induce complex changes within the blood vessel wall, acting with an oxidative[ncbi.nlm.nih.gov]

  • Methylmalonic Acidemia with Homocystinuria Type cblJ

    Other names of the condition: Methylmalonic acidemia and homocystinemia[xpertdox.com] Title Other Names: Methylmalonic acidemia and homocystinemia Categories: Subtypes: This disease is grouped under: Methylmalonic acidemia with homocystinuria is an inherited[rarediseases.info.nih.gov] A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. methylmalonic acidemia and homocystinemia methylmalonic acidemia and homocystinuria[ghr.nlm.nih.gov]

  • Acute Massive Pulmonary Embolism

    Chronic obstructive pulmonary disease Drug abuse (intravenous drugs) Drug-induced lupus anticoagulant Heart failure Hemolytic anemias Heparin-associated thrombocytopenia Homocystinemia[medical-dictionary.thefreedictionary.com]

  • Tryptophanemia

    (homocystinuria) homocystinemia type I homocystinemia type II homocystinemia type III methionine hypermethioninemia cystathioninemia cysteine/cystine cystinuria cystinosis[humpath.com] […] defects tyrosinemia type I tyrosinemia type II transient tyrosinemia of the newborn hawkinsinuria albinism alcaptonuria Sulfur-containing amino acids metabolism defects homocystinemia[humpath.com]

  • Anemia due to Glutathione Metabolism Disorder

    […] hydroxycobalamin, methionine, betaine Methylmalonic acidemia-homocystinuria (cblE; 236270) Methionine synthase reductase MTRR (5p15)* Biochemical profile: Homocystinuria, homocystinemia[merckmanuals.com] […] supplementation Methylenetetrahydrofolate reductase deficiency (236250) Methylenetetrahydrofolate reductase MTHFR (1p36.3)* Biochemical profile: Low to normal plasma methionine, homocystinemia[merckmanuals.com]

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