X-Linked Recessive Disease,Retinitis Pigmentosa,Connective Tissue Disease,Hyperuricemia,Purine-Pyrimidine Metabolic Disorder,Deafness, Autosomal Recessive 40,Urolithiasis,Tubulointerstitial Kidney Disease, Autosomal Dominant, 1,Movement Disease,Cataract 34, Multiple Types,Tetrahydrobiopterin Deficiency,Leukemia, Acute Lymphoblastic,Gout,Dystonia,Purine Nucleoside Phosphorylase Deficiency,Cockayne Syndrome,Aplastic Anemia,Colorectal Cancer,Parkinson Disease 1, Autosomal Dominant,Nephrolithiasis,Microcephaly,Cataract 4, Multiple Types,Teratocarcinoma,Deficiency Anemia,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Deafness, Autosomal Recessive 55,Skin Carcinoma,Disease Of Mental Health,Lesch-Nyhan Syndrome,Hyperuricemia, Hprt-Related,Myasthenic Syndrome, Congenital, 12,Retinitis Pigmentosa 23,Fragile X Syndrome,Phosphoribosylpyrophosphate Synthetase Superactivity,Inflammatory Bowel Disease,Nephrolithiasis, Uric Acid,X-Linked Monogenic Disease,Inflammatory Bowel Disease 16,Arts Syndrome,Hypothyroidism, Congenital, Nongoitrous, 6,Neuropathy, Hereditary Sensory And Autonomic, Type Viii,Adenine Phosphoribosyltransferase Deficiency,Immunodeficiency With Hyper-Igm, Type 1,Rett Syndrome,Ataxia-Telangiectasia,Bloom Syndrome

Purine-Pyrimidine Metabolic Disorder,Acute Laryngitis,Dissociative Amnesia,Lesch-Nyhan Syndrome