Metabolic nephropathies /nephrolithiasis

하단 표의 링크 버튼을 누르면 해당 카테고리의 포스트를 볼 수 있습니다.

Dent disease
Dent disease type 1 (CLCN5-related)Dent disease type 2 (OCRL-related)
Lowe syndrome
Lowe syndrome
Nephropathic cystinosis
Infantile nephropathic cystinosisJuvenile nephropathic cystinosis
Primary hyperoxaluria
Primary hyperoxaluria type 1 (PH1)Primary hyperoxaluria type 2 (PH2)Primary hyperoxaluria type 3 (PH3)
Cystinuria
CystinuriaHypotonia-cystinuria syndrome
Autosomal recessive infantile hypercalcemia
Autosomal recessive infantile hypercalcemia
Fabry disease
Fabry disease
Tubulopathy due to mitochondrial oxidative phosphorylation disorder
Tubulopathy due to mitochondrial oxidative phosphorylation disorder
Hereditary xanthinuria
Xanthinuria type IXanthinuria type II
Hypoxanthine-guanine phosphoribosyltransferase deficiency
Hypoxanthine-guanine phosphoribosyltransferase deficiency
Phosphoribosylpyrophosphate synthetase superactivity
Phosphoribosylpyrophosphate synthetase superactivity
LCAT deficiency
LCAT deficiency
Adenine phosphoribosyltransferase deficiency
Adenine phosphoribosyltransferase deficiency
Donnai-Barrow syndrome
Donnai-Barrow syndrome
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