Hepatocellular Carcinoma,Bardet-Biedl Syndrome 7,X-Linked Nonsyndromic Deafness,Arts Syndrome,Deafness, X-Linked 1,Charcot-Marie-Tooth Disease, X-Linked Recessive, 5

Brittle Bone Disorder,X-Linked Nonsyndromic Deafness,Deafness, X-Linked 1,Charcot-Marie-Tooth Disease, X-Linked Recessive, 5

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,Urolithiasis,Dihydroxyadeninuria,Morquio Syndrome,Congenital Muscular Dystrophy-Dystroglycanopathy Type A11,Mucopolysaccharidosis-Plus Syndrome,Cystinuria,Mucopolysaccharidosis Iv,Gout,Purine Nucleoside Phosphorylase Deficiency,Nephrolithiasis, Calcium Oxalate,Interstitial Nephritis,Nephrolithiasis,Hereditary Xanthinuria,Ureterolithiasis,Retinitis Pigmentosa 56,Lesch-Nyhan Syndrome,Lynch Syndrome,Phosphoribosylpyrophosphate Synthetase Superactivity,Arts Syndrome,Adenine Phosphoribosyltransferase Deficiency,Xanthinuria,Molybdenum Cofactor Deficiency, Complementation Group A,Mucopolysaccharidosis, Type Iva

Gastroesophageal Adenocarcinoma,Megaloblastic Anemia,Colorectal Cancer,Gastric Cancer,Arts Syndrome,Pyrimidine Metabolic Disorder,Adenine Phosphoribosyltransferase Deficiency,Charcot-Marie-Tooth Disease, X-Linked Recessive, 5,Orotic Aciduria,Postaxial Acrofacial Dysostosis

Charcot-Marie-Tooth Disease Type 5,Retinitis Pigmentosa,Hyperuricemia,Purine-Pyrimidine Metabolic Disorder,Neuromuscular Disease,X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome,Charcot-Marie-Tooth Disease X-Linked Recessive 4,Charcot-Marie-Tooth Neuropathy X Type 5,Dfnx1 Nonsyndromic Hearing Loss And Deafness,Sensorineural Hearing Loss,Hereditary Hearing Loss And Deafness,Fundus Dystrophy,Gout,Neuropathy,Charcot-Marie-Tooth Disease, Type 4b3,Charcot-Marie-Tooth Disease,X-Linked Charcot-Marie-Tooth Disease,X-Linked Non-Syndromic Sensorineural Deafness Type Dfn,Nonsyndromic Hearing Loss,Tooth Disease,Deafness, X-Linked 3,Deafness, X-Linked 4,Hutchinson-Gilford Progeria Syndrome,Lesch-Nyhan Syndrome,Deafness, X-Linked 5, With Peripheral Neuropathy,Phosphoribosylpyrophosphate Synthetase Superactivity,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Charcot-Marie-Tooth Disease Type X,X-Linked Nonsyndromic Deafness,Charcot-Marie-Tooth Disease, X-Linked Dominant, 6,Deafness, X-Linked 6,Ataxia, Combined Cerebellar And Peripheral, With Hearing Loss And Diabetes Mellitus,Nephrolithiasis, Uric Acid,Brown-Vialetto-Van Laere Syndrome,Arts Syndrome,Charcot-Marie-Tooth Disease, X-Linked Recessive, 2,Syndromic Intellectual Disability,Deafness, X-Linked 2,Deafness, X-Linked 1,Opitz-Kaveggia Syndrome,Syndromic X-Linked Intellectual Disability,Charcot-Marie-Tooth Disease, X-Linked Recessive, 5,Optic Atrophy, Hearing Loss, And Peripheral Neuropathy, Autosomal Recessive