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POLR3A-related disorder

MONDO:0700276

Disorder in which the cause of disease is a variation in the POLR3A gene.

2 clinical trials for this condition and its sub-types, 0 tagged with POLR3A-related disorder itself.

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Part of

↑ Hereditary disease (18187)

Sub-types of POLR3A-related disorder

Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism 2 trials
4 sub-types
- Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome 0 trials
- Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome 0 trials
- Odontoleukodystrophy 0 trials
- Tremor-ataxia-central hypomyelination syndrome 0 trials
Wiedemann-Rautenstrauch syndrome 0 trials

Including sub-types (2) Tagged with POLR3A-related disorder (0)

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