Tubular diseases

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

Primary Renal Tubular Acidosis
Proximal Renal Tubular Acidosis
Osteopetrosis with Renal Tubular Acidosis
Lowe syndrome
Dent's disease
Distal Renal Tubular Acidosis
Bartter syndrome
Gitelman syndrome
Hypokalemic alkalosis, CLDN10 associated
Genetic primary hypomagnesemia
Hypercalciuric hypomagnesemias
FHHNC type 1
FHHNC type 2
ADHH Bartter syndrome type 5
Bartter syndrome, type 3
Gitelman-like hypomagnesemias
Gitelman syndrome
Bartter syndrome, type 4
EAST syndrome
Isolated dominant hypomagnesemia
ADTKD/RCAD
HPABH4D/RCAD-like
Mitochondrial hypomagnesemias
Hypomagnesemia with secondary hypocalcemia
Hyperuricemia, pulmonary hypertension, renal failure and alkalotic syndrome
Kearns-Sayre syndrome
Other hypomagnesemias
Hypomagnesemia with secondary hypocalcemia
Isolated recessive hypomagnesemia
Neonatal inflammatory skin and bowel disease type 2
Hypomagnesemia with seizures and mental retardation
Autosomal dominant hypomagnesemia/episodic ataxia type 1
Kenny-Chaffey syndrome type 2
Nephrogenic Diabetes Insipidus
TubuloInterstitial Nephritis and Uveitis syndrome
Familial renal glucosuria
Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome
Autosomal dominant hypocalcemia
Hereditary renal hypouricemia
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