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Ichthyosis, congenital, autosomal recessive 12

MONDO:0015018

Any 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

10 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Ichthyosis (11) Hereditary skin disorder (5) Inherited ichthyosis (5) Disease of genetic or genomic mechanism (2) Autosomal recessive congenital ichthyosis (1) Disease by body system or component (0)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 2 Terminated 1
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