Ichthyosis, congenital, autosomal recessive 12
MONDO:0015018Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the CASP14 gene.
Also known as: ARCI12, ichthyosis, congenital, autosomal recessive 12, ichthyosis, congenital, autosomal recessive 12; ARCI12, ichthyosis, congenital, autosomal recessive type 12
3 clinical trials for this condition and its sub-types, 0 tagged with Ichthyosis, congenital, autosomal recessive 12 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.