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MIM:618688 - LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE; HLD19
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0032871 - leukodystrophy, hypomyelinating, 19, transient infantile |
DOID:0070400 - hypomyelinating leukodystrophy 19 |
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MONDO:0032871 - leukodystrophy, hypomyelinating, 19, transient infantile |
DOID:0070400 - hypomyelinating leukodystrophy 19 |