Inherited kidney disorder

A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system.

Identifiers: MONDO:0100191
Part of: Hereditary disease Kidney disorder
Also known as: genetic renal disease · inherited kidney disease · inherited renal disorder · nephrogenetic disorder

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Inherited renal tubular disease	MONDO:0015962	135
Familial nephrotic syndrome	MONDO:0002350	33
Familial cystic renal disease	MONDO:0019741	17
Hereditary nephritis	MONDO:0005334	12
Inherited pseudohypoaldosteronism	MONDO:0100323	11
Hereditary renal cell carcinoma	MONDO:0003008	9
Inherited focal segmental glomerulosclerosis	MONDO:0005363	9
Familial juvenile hyperuricemic nephropathy	MONDO:0000608	7
Renal agenesis	MONDO:0018470	7
Inherited distal renal tubular acidosis	MONDO:1060161	5
Liddle syndrome	MONDO:0008323	3
Congenital anomaly of kidney and urinary tract	MONDO:0019719	3
Fibronectin glomerulopathy	MONDO:0007671	2
Nephrolithiasis, calcium oxalate	MONDO:0957318	2
Renal tubular dysgenesis of genetic origin	MONDO:0009970	1
Alsing syndrome	MONDO:0021856
Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation	MONDO:0850089
Familial renal glucosuria	MONDO:0009297		SLC5A2
Hereditary kidney oncocytoma	MONDO:0003824
Hypophosphatemic nephrolithiasis/osteoporosis 1	MONDO:0012850		SLC34A1
Hypophosphatemic nephrolithiasis/osteoporosis 2	MONDO:0012851		NHERF1
Nephrolithiasis, X-linked recessive, with renal failure	MONDO:0010687		CLCN5
Neurohypophyseal diabetes insipidus	MONDO:0007450		AVP
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis	MONDO:0010644		CLCN5
Prune belly syndrome	MONDO:0007032		CHRM3

Rare disease

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