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Ichthyosis
MONDO:0019269Disorders of cornification that are characterized by visible scaling and/or hyperkeratosis of most or all of the skin. Inherited ichthyoses, defined as the generalized form of Mendelian disorders of cornification, affect most or all of the skin. This etiologically and phenotypically heterogenous group of conditions is caused by mutations in various different genes important for keratinocyte differentiation and epidermal barrier function. Acquired forms of ichthyosis can be observed with certain autoimmune, inflammatory, metabolic, endocrine, or infectious diseases or with malignancies.
Also known as: DOC, disorder of cornification, fish scale disease, fish skin disease, ichthyosis, ichthyosis (disease), non-syndromic ichthyosis
40 clinical trials for this condition and its sub-types, 13 tagged with Ichthyosis itself.
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Sub-types of Ichthyosis
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Inherited ichthyosis 6 trials · 32 incl. sub-types
13 sub-types
- Netherton syndrome 15 trials
- Autosomal recessive congenital ichthyosis 2 trials · 10 incl. sub-types Sub-types →
- Keratinopathic ichthyosis 0 trials · 7 incl. sub-types Sub-types →
- Ichthyosis vulgaris 3 trials Sub-types →
- Recessive X-linked ichthyosis 2 trials Sub-types →
- Peeling skin syndrome 1 trial Sub-types →
- IFAP syndrome 0 trials Sub-types →
- Congenital cataract-ichthyosis syndrome 0 trials
- Ichthyosis hystrix 0 trials Sub-types →
- Ichthyosis linearis circumflexa 0 trials
- Ichthyosis with erythrokeratoderma 0 trials
- Ichthyosis-oral and digital anomalies syndrome 0 trials
- Neonatal ichthyosis-sclerosing cholangitis syndrome 0 trials
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Acquired ichthyosis 0 trials
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Ichthyosis, follicular 0 trials