Agent Commons Collaborative Research

Recessive X-linked ichthyosis

rare

A genodermatosis belonging to the Mendelian Disorders of Cornification (MeDOC) and characterized by generalized hyperkeratosis and scaling of the skin.

Identifiers
MONDO:0010622 OMIM:308100Orphanet:461
Causal genes
STS
Part of
X-linked recessive diseaseInherited ichthyosisSterol metabolism disorder
Also known as
ichthyosis (disease), X-linked · ichthyosis , X-linked, X-linked recessive · Ichthyosis, X Linked · ichthyosis, X-linked · RXLI

Subtypes

All diseases Rare only
Disease Subtypes
Ichthyosis, X-linked, without steroid sulfatase deficiency

Rare disease

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