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Inherited ichthyosis

MONDO:0015947

Mendelian disorders of cornification affecting all or most of integument characterized by hyperkeratosis and/or scaling, caused by an inherited modification of the individual's genome.

Also known as: congenital ichthyosis of skin, genetic ichthyosis, hereditary ichthyosis (disease), inherited genetic ichthyosis, congenital ichthyosis, fish scale disease, fish skin, ichthyosis congenita

34 clinical trials for this condition and its sub-types, 6 tagged with Inherited ichthyosis itself.

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Sub-types of Inherited ichthyosis

Most studied deeper sub-types

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