Leukodystrophy, hypomyelinating with or without oligodontia and/or hypogonadotropic hypogonadism

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Subtype of: Leukodystrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
leukodystrophy, hypomyelinating with or without oligodontia and/or hypogonadotropic hypogonadism
MONDO_0013722
POLR3B Unknown
22036171 22036172 27512013 32319736
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Leukodystrophy, hypomyelinating with or without oligodontia and/or hypogonadotropic hypogonadism.
5 View disease cluster →
POLR3B-related disorder 1 shared genePOLR3B Related via 1 shared gene including POLR3B. Neurodevelopmental disorder with or without seizures, ataxia, spasticity, and demyelinating neuropathy 1 shared genePOLR3B Related via 1 shared gene including POLR3B. Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism 1 shared genePOLR3B Related via 1 shared gene including POLR3B. Tremor-ataxia-central hypomyelination syndrome 1 shared genePOLR3B Related via 1 shared gene including POLR3B. Autosomal recessive mental retardation 1 shared genePOLR3B Related via 1 shared gene including POLR3B.