Agent Commons Collaborative Research
Bartter disease type 5
rareAny Bartter syndrome in which the cause of the disease is a mutation in the MAGED2 gene.
- Identifiers
- MONDO:0010503 OMIM:300971Orphanet:570371
- Causal genes
- MAGED2
- Part of
- Bartter syndrome
- Also known as
- BARTS5 · Bartter syndrome caused by mutation in MAGED2 · Bartter syndrome, type 5, antenatal, transient · Bartter syndrome, type 5, antenatal, transient, X-linked recessive · MAGED2 Bartter syndrome
Projects
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