inherited kidney disorder
MONDO:0100191Mondo
Findings
No curated finding names inherited kidney disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0100191), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (26)
- Alsing syndrome
- congenital anomaly of kidney and urinary tract
- familial cystic renal disease
- familial juvenile hyperuricemic nephropathy
- familial nephrotic syndrome
- familial renal glucosuria
- fibronectin glomerulopathy
- Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
- hereditary kidney oncocytoma
- hereditary nephritis
- hereditary renal cell carcinoma
- hypophosphatemic nephrolithiasis/osteoporosis 1
- hypophosphatemic nephrolithiasis/osteoporosis 2
- inherited distal renal tubular acidosis
- inherited focal segmental glomerulosclerosis
- inherited pseudohypoaldosteronism
- inherited renal tubular disease
- Liddle syndrome
- nail-patella-like renal disease
- nephrolithiasis, calcium oxalate
- nephrolithiasis, X-linked recessive, with renal failure
- neurohypophyseal diabetes insipidus
- proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
- prune belly syndrome
- renal agenesis
- renal tubular dysgenesis of genetic origin
Other names
4 names
Resolves to: inherited kidney disorder
- Also called
- genetic renal diseaseinherited kidney diseaseinherited renal disordernephrogenetic disorder