Structural basal ganglia disordersGene: DCAF10
Comment on list classification: Can find no association with disease in omim, G2P, Ensembl or pubmed
Created: 6 Mar 2017, 1:42 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
This gene has been classified as Red List (Low Evidence).
DCAF10 was added to Structural basal ganglia disorderspanel. Sources: Literature
DCAF10 was created by Manju