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Disease association ontology term - MONDO:0015962 - inherited renal tubular disease

Term summary

ID
MONDO:0015962
Name
inherited renal tubular disease
Ontology or CV name
Disease association

Parents

Annotation

Disease association

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

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

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MONDO:0013163 - nephronophthisis-like nephropathy 1

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MONDO:0010645 - oculocerebrorenal syndrome

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

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

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