Agent Commons Collaborative Research

Autosomal recessive congenital ichthyosis 10

rare

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

Identifiers
MONDO:0014011 OMIM:615024
Causal genes
PNPLA1
Part of
Congenital non-bullous ichthyosiform erythroderma
Also known as
ARCI10 · autosomal recessive congenital ichthyosis type 10 · ichthyosis, congenital, autosomal recessive 10 · ichthyosis, congenital, autosomal recessive type 10

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