hereditary hyperbilirubinemia

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• Hereditary hyperbilirubinemia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD10|E|80|4|e|70 ICD10|E|80|6|e|70 ICD9 = ICD9|277.4 ICDO = OMIM = MedlinePlus = eMedicineSubj = med eMedicineTopic = 1065 eMedicine mult = eMedicine2|med|1066 | MeshID = D006933… …   Wikipedia

• Hereditary coproporphyria — Classification and external resources Coproporphyrinogen III ICD 10 E …   Wikipedia

• Hereditary spherocytosis — This article is about aspects of spherocytosis specific to the hereditary form of the disorder. For details that apply generally to this variant as well as others, see Spherocytosis. Hereditary spherocytosis Classification and external resources… …   Wikipedia

• Hereditary 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… …   Medical dictionary

• HS (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… …   Medical dictionary

• Spherocytosis, 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… …   Medical dictionary

• Crigler–Najjar syndrome — Classification and external resources Bilirubin ICD 10 E80.5 …   Wikipedia

• Dubin–Johnson syndrome — Dubin Johnson syndrome Classification and external resources Bilirubin ICD 10 E80.6 …   Wikipedia

• Porphyria — This article is about the medical condition. For other uses, see Porphyry (disambiguation). Porphyria Classification and external resources ICD 10 E80.0 E80.2 …   Wikipedia

• Kernicterus — ICDO = OMIM = MedlinePlus = 003243 eMedicineSubj = ped eMedicineTopic = 1247 MeshID = D007647 Kernicterus is damage to the brain centers of infants caused by increased levels of unconjugated indirect bilirubin which is free (not bound to albumin) …   Wikipedia

• Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 …   Wikipedia