normal life expectancy
21Congenital 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 …
22Deficiency, 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… …
23Hemolytic jaundice, congenital — 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 …
24Hereditary spherocytosis (HS) — 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, and more fragile than normal. The red cells have a… …
25HS (hereditary spherocytosis) — 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, and more fragile than normal. The red cells have a… …
26Jaundice, congenital hemolytic — 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 …
27Spherocytosis, hereditary (HS) — 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, and more fragile than normal. The red cells have a… …
28alkaptonuria — /al kap teuh noor ee euh, nyoor /, n. Pathol. excessive excretion of homogentisic acid in the urine, caused by a hereditary abnormality of the metabolism of tyrosine and phenylalanine. [1885 90; ALKAPTON + URIA] * * * ▪ pathology rather… …
29Relay — This article is about the electrical component. For other uses, see Relay (disambiguation). Automotive style miniature relay, dust cover is taken off A relay is an electrically operated switch. Many relays use an electromagnet to operate a… …
30Tethered spinal cord syndrome — Classification and external resources ICD 10 Q06.8 ICD 9 742.59 …
