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Summary Literature (0)
MIM:618006 - LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17

Xenbase Genes: aimp2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054817 - leukodystrophy, hypomyelinating, 17

Disease Ontology (DO):
DOID:0070404 - hypomyelinating leukodystrophy 17