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Disease association ontology term - MONDO:0100191 - inherited kidney disorder

Term summary

ID
MONDO:0100191
Name
inherited kidney disorder
Ontology or CV name
Disease association
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.

Parents

Annotation

Disease association

MONDO:0018965 - Alport syndrome

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Genes:

MONDO:0014937 - aniridia 2

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Genes:

MONDO:0008368 - autosomal dominant distal renal tubular acidosis

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MONDO:0011422 - autosomal recessive proximal renal tubular acidosis

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MONDO:0979883 - cranioectodermal dysplasia 6

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MONDO:0009067 - cystinuria

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MONDO:0015612 - Dent disease

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MONDO:0010225 - Dent disease type 1

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MONDO:0010359 - Dent disease type 2

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MONDO:0019006 - familial idiopathic steroid-resistant nephrotic syndrome

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MONDO:0000608 - familial juvenile hyperuricemic nephropathy

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MONDO:0013836 - familial steroid-resistant nephrotic syndrome with sensorineural deafness

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MONDO:0011303 - focal segmental glomerulosclerosis 1

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MONDO:0013589 - focal segmental glomerulosclerosis 6

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MONDO:0014462 - focal segmental glomerulosclerosis 8

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MONDO:0003789 - hereditary papillary renal cell carcinoma

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MONDO:0013458 - hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome

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MONDO:0014891 - hyperuricemic nephropathy, familial juvenile type 4

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MONDO:0859328 - hypomagnesemia 7, renal, with or without dilated cardiomyopathy

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MONDO:0013898 - karyomegalic interstitial nephritis

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MONDO:0008323 - Liddle syndrome

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MONDO:0020722 - nephrolithiasis susceptibility caused by SLC26A1

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MONDO:0010687 - nephrolithiasis, X-linked recessive, with renal failure

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MONDO:0013163 - nephronophthisis-like nephropathy 1

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MONDO:0014752 - nephrotic syndrome, type 11

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MONDO:0014817 - nephrotic syndrome, type 12

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MONDO:0014818 - nephrotic syndrome, type 13

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MONDO:0032580 - nephrotic syndrome, type 17

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MONDO:0032581 - nephrotic syndrome, type 18

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MONDO:0032582 - nephrotic syndrome, type 19

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MONDO:0026726 - nephrotic syndrome, type 20

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MONDO:0014099 - nephrotic syndrome, type 8

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MONDO:0014257 - nephrotic syndrome, type 9

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MONDO:0010645 - oculocerebrorenal syndrome

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MONDO:0010916 - polycystic kidney disease 3 with or without polycystic liver disease

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MONDO:0031062 - polycystic kidney disease 7

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MONDO:0010644 - proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis

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MONDO:0013782 - pseudohypoaldosteronism type 2E

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MONDO:0011301 - pseudohypoparathyroidism type 1B

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MONDO:0044726 - psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome

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MONDO:0009968 - renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss

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MONDO:0011268 - renal tubular acidosis, distal, 3, with or without sensorineural hearing loss

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MONDO:0012700 - renal tubular acidosis, distal, 4, with hemolytic anemia

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MONDO:0054565 - short-rib thoracic dysplasia 17 with or without polydactyly

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