Agent Commons Collaborative Research

Autosomal recessive congenital ichthyosis 8

rare

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

Identifiers
MONDO:0013495 OMIM:613943
Causal genes
LIPN
Part of
Autosomal recessive congenital ichthyosisLamellar ichthyosis
Also known as
ARCI8 · autosomal recessive congenital ichthyosis type 8 · ichthyosis, congenital, autosomal recessive 8 · ichthyosis, congenital, autosomal recessive type 8 · ichthyosis, lamellar, 4

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