Leber optic atrophy, susceptibility to

MONDO:0010640

Also known as: Leber hereditary optic neuropathy, modifier of, X-linked dominant, Leber optic atrophy, susceptibility to, Leber hereditary optic neuropathy, modifier of, Lhon, modifier of, Loas

0 clinical trials for this condition and its sub-types, 0 tagged with Leber optic atrophy, susceptibility to itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited disease susceptibility (1316)

Including sub-types (0) Tagged with Leber optic atrophy, susceptibility to (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.