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Lamellar ichthyosis

MONDO:0017778

A keratinization disorder characterized by the presence of large scales all over the body without significant erythroderma.

Also known as: LI, classic lamellar ichthyosis, congenital lamellar ichthyosis

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

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Sub-types

Autosomal recessive congenital ichthyosis 6 (1) Autosomal recessive congenital ichthyosis 3 (0) Autosomal recessive congenital ichthyosis 4A (0) Autosomal recessive congenital ichthyosis 4B (0) Autosomal recessive congenital ichthyosis 5 (0) Autosomal recessive congenital ichthyosis 8 (0) Ichthyosis, lamellar, autosomal dominant (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Human disease (14) Hereditary skin disorder (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Disease by body system or component (0)
Trials to join now! 11 Not yet recruiting 2 Not yet finished but already full! 3 Completed 3 Terminated 1
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