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MIM:616494 - LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11
Xenbase Genes: polr1c
Human Disease Resource: MIM
MONDO:0014666 - hypomyelinating leukodystrophy 11 |
MONDO:0019505 - obsolete hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome |