Wolfram syndrome 2

MONDO:0011502

Any Wolfram syndrome in which the cause of the disease is a mutation in the CISD2 gene.

Also known as: CISD2 Wolfram syndrome, WFS2, Wolfram syndrome 2, Wolfram syndrome caused by mutation in CISD2, Wolfram syndrome type 2, WOLFRAM syndrome 2

0 clinical trials for this condition and its sub-types, 0 tagged with Wolfram syndrome 2 itself.

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Part of

↑ Hereditary disease (18187) ↑ Wolfram syndrome (7)

Including sub-types (0) Tagged with Wolfram syndrome 2 (0)

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