Fanconi renotubular syndrome 3

MONDO:0014275

Any Fanconi syndrome in which the cause of the disease is a mutation in the EHHADH gene.

Also known as: EHHADH Fanconi syndrome, Fanconi renotubular syndrome 3, Fanconi renotubular syndrome type 3, Fanconi syndrome caused by mutation in EHHADH, FRTS3

1 clinical trial for this condition and its sub-types, 0 tagged with Fanconi renotubular syndrome 3 itself.

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Where it sits in the disease tree

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Part of

↑ Primary Fanconi syndrome (0)

Including sub-types (1) Tagged with Fanconi renotubular syndrome 3 (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC

Fanconi renotubular syndrome 3

Where it sits in the disease tree

Could a diabetes drug protect kidneys in children with genetic disease?