UMR 5199 PACEA

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Morphology in Oral Rare Syndromes & Artificial Intelligence for Clinical Diagnosis	Bone Diseases, Developmental, Bone Diseases, Metabolic, Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hypophosphatemia, Familial, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Stomatognathic Diseases, Stomatognathic System Abnormalities, Tooth Abnormalities, Urogenital Diseases, X-linked hypophosphatemic rickets, bone disorder, calcium metabolic disease, connective tissue disorder, cutaneous mucinosis, hereditary disease, hypophosphatemia, hypophosphatemic rickets, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn metal metabolism disorder, kidney disorder, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, musculoskeletal system disorder, nutritional deficiency disease, nutritional disorder, osteochondrodysplasia, osteogenesis imperfecta, phosphorus metabolism disease, renal tubular transport disease, rickets, tooth disorder, urinary system disorder, vitamin D deficiency, vitamin deficiency disorder	Not yet recruiting	Not applicable	2026-06-24		NCT07666269

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