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Contents

Synopsis Codes Differential Diagnosis & Pitfalls Best Tests References

Autosomal dominant tubulointerstitial kidney disease

Contents

Synopsis Codes Differential Diagnosis & Pitfalls Best Tests References

Other Resources UpToDate PubMed

Important News & Links

Autosomal dominant tubulointerstitial kidney disease

Contributors: Catherine Moore MD

Other Resources UpToDate PubMed

Alerts and Notices

Important News & Links

Synopsis

Autosomal dominant tubulointerstitial kidney disease : Fatigue, Creatinine elevated, Hyperuricemia, Polyuria, Polydipsia, BP increased, RBC decreased

A rare autosomal dominant disorder characterized by progressive renal impairment with bland urine sediment. Medullary cysts may be seen on ultrasound but are more commonly not present.

Codes

ICD10CM:
Q61.5 – Medullary cystic kidney

SNOMEDCT:
204957003 – Medullary cystic disease

Differential Diagnosis & Pitfalls

To perform a comparison, select diagnoses from the classic differential

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Best Tests

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References

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Last Updated:01/11/2022

Autosomal dominant tubulointerstitial kidney disease

A medical illustration showing key findings of Autosomal dominant tubulointerstitial kidney disease : Fatigue, Creatinine elevated, Hyperuricemia, Polyuria, Polydipsia, BP increased, RBC decreased

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