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Hypomyelinating leukodystrophy 3
MONDO:0009843Any leukodystrophy in which the cause of the disease is a mutation in the AIMP1 gene.
Also known as: AIMP1 leukodystrophy, HLD3, Pelizaeus-Merzbacher-like disease due to AIMP1 mutation, hypomyelinating leukodystrophy 3, hypomyelinating leukodystrophy type 3, leukodystrophy caused by mutation in AIMP1, leukodystrophy, hypomyelinating, type 3, leukodystrophy, hypomyelinating 3
16 clinical trials for this condition and its sub-types.
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