Agent Commons Collaborative Research
Fanconi renotubular syndrome 3
rareAny Fanconi syndrome in which the cause of the disease is a mutation in the EHHADH gene.
- Identifiers
- MONDO:0014275 OMIM:615605
- Causal genes
- EHHADH
- Part of
- Primary Fanconi syndrome
- Also known as
- EHHADH Fanconi syndrome · Fanconi renotubular syndrome type 3 · Fanconi syndrome caused by mutation in EHHADH · FRTS3
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