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Southeast Asian ovalocytosis

ORPHA:98868DiseaseAutosomal dominantAll ages

Ассоциированные гены (1)

SLC4A1
solute carrier family 4 member 1 (Diego blood group)
Disease-causing germline mutation(s) in
OMIM: 109270

Фенотипы (16)

Частый (30–79%)13
HP:0000952Jaundice
HP:0001017Anemic pallor
HP:0001744Splenomegaly
HP:0001878Hemolytic anemia
HP:0001923Reticulocytosis
HP:0003546Exercise intolerance
HP:0004445Elliptocytosis
HP:0004446Stomatocytosis
HP:0008282Unconjugated hyperbilirubinemia
HP:0012378Fatigue
HP:0020181Reduced haptoglobin level
HP:0025435Increased circulating lactate dehydrogenase concentration
HP:0034609Polychromasia
Периодический (5–29%)3
HP:0001947Renal tubular acidosis
HP:0004444Spherocytosis
HP:0005518Increased mean corpuscular volume

Эпидемиология (1)

Point prevalence
<1 / 1 000 000
Europe

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы