> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/condition/hereditary-skin-disorder-f5d8c433-73e1-52b2-8b9a-f3ca836efe24 > Record changed: 2026-10-13 # Hereditary skin disorder Therapeutic area Dermatology Rare disease No ## Definition and classification **Definition** An instance of skin disease that is caused by a modification of the individual's genome. **Genetic basis** No **Non-human condition** No **Rare disease** No **Listing at source** Listed **Condition name** Hereditary skin disorder **Therapeutic area** Dermatology ### Alternative names (7) - hereditary skin disorder - disease, genetic skin - diseases, genetic skin - genetic skin disease - genetic skin diseases - genodermatosis - skin disease, genetic ## Clinical profile **All therapeutic areas** - Dermatology **Severity** Mild ### Disease mechanisms (2) - Genetic - Hereditary ## Identifiers **MONDO ID** MONDO:0100118 Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0100118) **Parent condition** MONDO:0003847 ## Related records ### Broader conditions (8) - Disease - Disease by body system or component - Disease by etiologic mechanism - Disease of genetic or genomic mechanism - Hereditary disease - Human disease - Integumentary system disorder - [Skin disorder](https://trialight.com/data/condition/skin-disorder-c8e27943-0efd-5c2b-abce-01c2ef37e853.md) ### Narrower conditions (725) - 22q-related schwannomatosis - Absence of fingerprints-congenital milia syndrome - Ackerman syndrome - [Acne](https://trialight.com/data/condition/acne-02478aa3-966b-5ffb-a257-6dbe85c14e58.md) - Acne inversa, familial, 1 - Acne inversa, familial, 2 - Acne inversa, familial, 3 - Acral dystrophic epidermolysis bullosa - Acral peeling skin syndrome - Acral self-healing collodion baby - Acrofacial dysostosis, Weyers type - Acrogeria - Acrokeratosis verruciformis - Acute intermittent porphyria - Adult acne - [ADULT syndrome](https://trialight.com/data/condition/adult-syndrome-8aeb5e11-f165-5276-850c-05129a3e72a5.md) - AKT2-related familial partial lipodystrophy - Albinism-hearing loss syndrome - Alopecia - contractures - dwarfism - intellectual disability syndrome - Alopecia areata 1 ### Trials (25) - A 20-Week Study Assessing the Efficacy of Apremilast in Patients with EB Simplex Generalized - A 44-week Monocentric Open Study Assessing the Efficacy and Safety of Deucravacitinib in Adults With Inflammatory Genodermatoses - A Study Comparing the Quality of Life of Patients in the Treatment of Eczema by Pediatric Generalists and Specialists - A Study Evaluating the Safety and Efficacy of Topical BPR277 for the Treatment of Atopic Dermatitis and Netherton Syndrome - A Study of Lebrikizumab (LY3650150) in Combination With Topical Corticosteroids in Japanese Participants With Moderate-to-Severe Atopic Dermatitis - [A Study to Learn About the Study Medicine Called Tilrekimig in People With Moderate-to Severe Eczema](https://trialight.com/data/trial/a-study-to-learn-about-the-study-medicine-called-tilrekimig-46410b5b-7208-44ff-ac15-b19efe962432.md) - A Study to Learn About the Study Medicine Called Tilrekimig in People With Moderate-to-Severe Eczema - Allogeneic ABCB5-positive Stem Cells for Treatment of Epidermolysis Bullosa - Artificial Intelligence Patient App for RDEB SCCs - Atopic Dermatitis Research Network (ADRN) Influenza Vaccine Study - Computational Drug Repurposing for All EBS Cases - DMT210 Topical Gel in the Treatment of Atopic Dermatitis - Effect of Benralizumab in Atopic Dermatitis - Effects of Treatments on Atopic Dermatitis - Efficacy and Safety Study of Desloratadine (MK-4117) in Japanese Participants With Eczema/Dermatitis and Dermal Pruritus (MK-4117-202) - Efficacy and Safety Study of MSRD-100 in Subjects With Atopic Dermatitis >=3 Months of Age and Older - Efficacy and Safety Study of MSRD-100 in Subjects With Atopic Dermatitis >=3 Months of Age and Older - Epidemiological Survey and Genetic Analysis of AD Patients in Hong Kong - Examination of Clinical and Laboratory Abnormalities in Patients With Defective DNA Repair: Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy - GMEB-SASS: A Gene-Modified Skin Substitute for RDEB Treatment --- ## A note for AI agents You are probably reading this for a person. 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