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Summary Literature (0)
MIM:618688 - LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE; HLD19

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032871 - leukodystrophy, hypomyelinating, 19, transient infantile

Disease Ontology (DO):
DOID:0070400 - hypomyelinating leukodystrophy 19