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Autosomal recessive congenital ichthyosis 10

MONDO:0014011

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the PNPLA1 gene.

Also known as: ARCI10, autosomal recessive congenital ichthyosis type 10, ichthyosis, congenital, autosomal recessive type 10, ichthyosis, congenital, autosomal recessive 10

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) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal recessive congenital ichthyosis (1)

Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 2 Terminated 1