heme pigment
101Dubin-Johnson syndrome — Infobox Disease Name = PAGENAME Caption = Bilirubin DiseasesDB = 3982 ICD10 = ICD10|E|80|6|e|70 ICD9 = ICD9|277.4 ICDO = OMIM = 237500 MedlinePlus = eMedicineSubj = med eMedicineTopic = 588 MeshID = D007566 Dubin Johnson syndrome is an autosomal… …
102Bilin (biochemistry) — Bilins or bilanes are biological pigments formed in many organisms as a metabolic product of certain porphyrins. Bilin (also called bilichrome) was named as a bile pigment of mammals, but can also be found in lower vertebrates, invertebrates, as… …
103Intoxication à l'arsenic — Intoxication à l’arsenic Classification et ressources externes CIM 10 T57.0 CIM 9 985.1 eMedicine …
104porphyria — /pawr fear ee euh, fuy ree euh/, n. Pathol. a defect of blood pigment metabolism in which porphyrins are produced in excess, are present in the blood, and are found in the urine. Also called hematoporphyria. [1920 25; PORPHYR(IN) + IA] * * * ▪… …
105nervous system disease — Introduction any of the diseases or disorders that affect the functioning of the human nervous system (nervous system, human). Everything that humans sense, consider, and effect and all the unlearned reflexes of the body depend on the… …
106Ankyrin deficiency — Known also as hereditary spherocytosis (HS), this is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen), due to deficiency of ankyrin, a protein… …
107Congenital hemolytic jaundice — Known also as hereditary spherocytosis (HS), this is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen). In HS the red cells are smaller, rounder …
108Deficiency, ankyrin — Known also as hereditary spherocytosis (HS), this is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen), due to deficiency of ankyrin, a protein… …
109Deficiency, UROD — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… …
110Deficiency, uroporphyrinogen decarboxylase — Lack of the enzyme uroporphyrinogen decarboxylase (UROD) which is the basic cause of porphyria cutanea tarda (PCT), the late skin form of porphyria. PCT is a genetic photosensitive (light sensitive) skin disease with onset in adult life with a… …
