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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

37 clinical trials for this condition and its sub-types.

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Sub-types

Netherton syndrome (13) Superficial epidermolytic ichthyosis (6) Ichthyosis vulgaris (3) Autosomal recessive congenital ichthyosis 1 (2) Recessive X-linked ichthyosis (2) Autosomal recessive congenital ichthyosis (1) Autosomal recessive congenital ichthyosis 6 (1) Epidermolytic ichthyosis (1) Peeling skin syndrome (1) Acral peeling skin syndrome (0) Acral self-healing collodion baby (0) Annular epidermolytic ichthyosis (0) Autosomal dominant epidermolytic ichthyosis (0) Autosomal dominant ichthyosis vulgaris (0) Autosomal recessive congenital ichthyosis 10 (0) Autosomal recessive congenital ichthyosis 11 (0) Autosomal recessive congenital ichthyosis 2 (0) Autosomal recessive congenital ichthyosis 3 (0) Autosomal recessive congenital ichthyosis 4A (0) Autosomal recessive congenital ichthyosis 4B (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Ichthyosis (11) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Epidermal disease (0)

Trials to join now! 10 Not yet recruiting 7 Not yet finished but already full! 4 Completed 12 Terminated 4