POLR3A-related disorder
MONDO:0700276Disorder in which the cause of disease is a variation in the POLR3A gene.
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism
(2)
Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome
(0)
Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome
(0)
Odontoleukodystrophy
(0)
Tremor-ataxia-central hypomyelination syndrome
(0)
Wiedemann-Rautenstrauch syndrome
(0)