cystathionine β-synthetase
31Arylformamidase — Identifiers EC number 3.5.1.9 CAS number 156229 75 3 …
32Methionine synthase — 5 methyltetrahydrofolate homocysteine methyltransferase PDB rendering based on 2o2k …
33Cystathioninuria — Classification and external resources Cystathionine ICD 10 E …
34Liste des maladies génétiques à gène identifié — Ceci est la liste des maladies génétiques à gène identifié. Voir aussi la : liste des maladies génétiques à gène non identifié. Les maladies génétiques citées ici sont les maladies génétiques dont le gène est connu (Symbole + de MIM) ou dont …
35Homocysteine — An amino acid produced by the body, usually as a byproduct of consuming meat. Homocysteine is made from another amino acid, methionine, and then in turn is converted into other amino acids. Elevated levels of homocysteine in the blood appear to… …
36homocystinuria — ▪ pathology hereditary metabolic disorder involving methionine, a sulfur containing essential amino acid. The metabolic sequence of methionine normally begins with its stepwise conversion to homocysteine, cystathionine, and cysteine,… …
37List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… …
38connective tissue disease — Introduction any of the diseases that affect human connective tissue. Diseases of the connective tissue can be divided into (1) a group of relatively uncommon genetic disorders (genetic disease, human) that affect the primary structure of… …
39Arginine — L Arginine IUPAC name …
40Chromosome 21 (human) — Chromosome 21 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. The trisomy of the 21st chromosome causes Down Syndrome. Chromosome 21 is the smallest human chromosome, 47 million nucleotides… …
