Congenital Aphakia,Hereditary Spastic Paraplegia,Parkinson Disease 20, Early-Onset,Hermansky-Pudlak Syndrome,Macrocephaly/Autism Syndrome,Niemann-Pick Disease, Type C1,Joubert Syndrome 1

Microcephaly And Chorioretinopathy 1,Exophthalmos,Teeth Hard Tissue Disease,Amelogenesis Imperfecta,Nevus, Epidermal,Noonan Syndrome 1,Phosphorus Metabolism Disease,Choanal Atresia, Posterior,Gingival Hypertrophy,Osteoglophonic Dysplasia,Caffey Disease,Osteomalacia,Microcephaly,Coloboma, Ocular, With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation,Mineral Metabolism Disease,Hypophosphatemia,Arterial Calcification Of Infancy,Hypophosphatemic Rickets, Autosomal Dominant,Autosomal Recessive Hypophosphatemic Rickets,Hypophosphatemic Rickets, X-Linked Dominant,Amelogenesis Imperfecta, Type Ig,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Osteogenesis Imperfecta, Type Iii,Raine Syndrome

Acrodysostosis 1 With Or Without Hormone Resistance,Jalili Syndrome,Immunodeficiency 9,Teeth Hard Tissue Disease,Amelogenesis Imperfecta,Superficial Keratitis,Carney Complex, Type 1,Nephrocalcinosis,Carney Complex Variant,Hypoplastic Amelogenesis Imperfecta,Dental Pulp Calcification,Acrodysostosis With Multiple Hormone Resistance,Gingival Overgrowth,Amelogenesis Imperfecta Hypoplastic Type, Ig,Acrodysostosis,Gingival Disease,Pigmented Nodular Adrenocortical Disease, Primary, 1,Tooth Agenesis,Trichodentoosseous Syndrome,Primary Pigmented Nodular Adrenocortical Disease,Amelogenesis Imperfecta, Type Ig,Gingival Fibromatosis,Myxoma, Intracardiac