xeroderma pigmentosum
xeroderma pigmentosum
Explore linked clinical trials. Standard reference: MONDO:00196002 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History Study for DNA Repair Disorders | Abnormalities, Multiple, Bone Diseases, Developmental, Cockayne syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Dwarfism, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, Trichothiodystrophy Syndromes, bone disorder, hereditary disease, hereditary skin disorder, inherited neurodegenerative disorder, metabolic disease, musculoskeletal system disorder, neoplasm, nervous system disorder, neurodegenerative disease, photosensitivity disease, precancerous condition, skin disorder, skin pigmentation disorder, xeroderma pigmentosum | Recruiting | Not stated | 2026-05-27 | NCT05484570 | |
| Reproductive Options in Inherited Skin Diseases | Abnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, DNA repair disease, Eye Diseases, Hereditary, Infant, Newborn, Diseases, Jaw Cysts, Jaw Diseases, Keratoderma, Palmoplantar, Malformations of Cortical Development, Group I, Neoplasms by Histologic Type, Neoplasms, Multiple Primary, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, Stomatognathic Diseases, albinism, basal cell carcinoma, basal cell neoplasm, bone disorder, carcinoma, central nervous system malformation, cerebral cortical dysplasia, connective tissue disorder, cutis laxa, ectodermal dysplasia syndrome, epidermolysis bullosa, epithelial neoplasm, eye disorder, hamartoma, hereditary disease, hereditary neoplastic syndrome, hereditary skin disorder, hypopigmentation of the skin, ichthyosis, inborn disorder of amino acid metabolism, inborn errors of metabolism, inherited neurodegenerative disorder, keratosis, metabolic disease, musculoskeletal system disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, nevoid basal cell carcinoma syndrome, odontogenic cyst, photosensitivity disease, precancerous condition, skin disorder, skin pigmentation disorder, solitary bone cyst, tuberous sclerosis, vesiculobullous skin disease, xeroderma pigmentosum | Enrolling by invitation | Not stated | 2025-05-18 | NCT06330324 |