Hereditary metabolic kidney disease

Metabolic kidney disease is a wide group of disorders that are characterized of metabolic disturbances which result in kidney symptoms.

Systematic

Hereditary kidney diseases
	Congenital abnormalities of the kidney and urinary tract
	Cystic kidney disease
	Disorders of tubular solute transport
	Hereditary glomerular disease
	Hereditary metabolic kidney disease
		Fabry disease
			GLA
		Hereditary amyloidosis
			ATTR amyloidosis
				TTR
			Amyloidosis, cerebroarterial
				Amyloidosis, cerebroarterial, Britisch type
					ITM2B
				Amyloidosis, cerebroarterial, Danish type
					ITM2B
				Amyloidosis, cerebroarterial, Dutch type
					APP
				Amyloidosis, cerebroarterial, Icelandic type
					CST3
			Cryopyrin-associated periodic syndrome
				CINCA syndrome
					NLRP3
				Familial cold autoinflammatory syndrome 1
					NLRP3
				Muckle-Wells syndrome
					NLRP3
			Familial mediterranean fever
				MEFV
				NOD2
				SAA1
				TNFRSF1A
			Finnish type Amyloidosis
				GSN
			Hereditary renal amyloidosis
				APOA1
				Apolipoprotein A-2 amyloidosis
					APOA2
				B2M
				CST3
				FGA
				LYZ
		Hyperoxaluria
			Hyperoxaluria type 1
				AGXT
			Hyperoxaluria type 2
				GRHPR
			Hyperoxaluria type 3
				HOGA1
		Lysinuric protein intolerance
			SLC7A7
	Hereditary renal tumors
	Interstitial kidney disease
	Kidney disease appearing as endocrinological disorders
	Thrombotic microangiopathies
	Urolithiasis

Update:

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