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Hereditary renal hypouricemia

ORPHA:94088Malformation syndromeAutosomal recessiveAll ages

Ассоциированные гены (2)

SLC22A12
solute carrier family 22 member 12
Disease-causing germline mutation(s) (loss of function) in
OMIM: 607096
SLC2A9
solute carrier family 2 member 9
Disease-causing germline mutation(s) (loss of function) in
OMIM: 606142

Фенотипы (16)

Облигатный (100%)2
HP:0003149Hyperuricosuria
HP:0003537Hypouricemia
Очень частый (80–99%)1
HP:0030973Postexertional malaise
Частый (30–79%)4
HP:0000091Abnormal renal tubule morphology
HP:0001919Acute kidney injury
HP:0008651Uric acid urolithiasis independent of gout
HP:0012211Abnormal renal physiology
Периодический (5–29%)9
HP:0000790Hematuria
HP:0002013Vomiting
HP:0002018Nausea
HP:0002150Hypercalciuria
HP:0003138Increased blood urea nitrogen
HP:0003418Back pain
HP:0012213Decreased glomerular filtration rate
HP:0012595Mild proteinuria
HP:0012622Chronic kidney disease

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы