X-Linked Recessive Disease,Medullary Sponge Kidney,Nephrotic Syndrome,Bethlem Myopathy 1,Bartter Disease,Renal Tubular Transport Disease,Myotonia Congenita,Nephrocalcinosis,Idiopathic Hypercalciuria,Cystic Fibrosis,Nephronophthisis,Cataract,Cystinuria,Ureteral Obstruction,Night Blindness,Donnai-Barrow Syndrome,Kidney Disease,Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak,Nephrolithiasis, Calcium Oxalate,Osteomalacia,Rickets,Fanconi Syndrome,Aminoaciduria,Nephrolithiasis,Dent Disease 1,Hypophosphatemic Rickets, X-Linked Recessive,Hypophosphatemia,X-Linked Monogenic Disease,Proteinuria, Low Molecular Weight, With Hypercalciuria And Nephrocalcinosis,Lowe Oculocerebrorenal Syndrome,Nephrolithiasis, X-Linked Recessive, With Renal Failure

Lens Subluxation,Vascular Disease,Homocystinuria,Homocystinuria Caused By Cystathionine Beta-Synthase Deficiency,Malignant Hyperthermia,Familial Hypercholesterolemia,Methylmalonic Aciduria And Homocystinuria, Cblc Type,Homocystinuria Due To Cystathionine Beta-Synthase Deficiency,Neural Tube Defects,Hypermethioninemia,Down Syndrome,Glycine N-Methyltransferase Deficiency,Wolff-Parkinson-White Syndrome,Methionine Adenosyltransferase I/Iii Deficiency,Marfan Syndrome

Senior-Loken Syndrome 1,Retinitis Pigmentosa,Pseudoretinitis Pigmentosa,Leber Congenital Amaurosis 9,Pathologic Nystagmus,Eye Degenerative Disease,Leber Plus Disease,Retinal Degeneration,Fundus Dystrophy,Keratoconus,Retinal Disease,Usher Syndrome, Type I,Usher Syndrome, Type Iiia,Stargardt Disease,Cone-Rod Dystrophy 2,Retinitis,Leber Congenital Amaurosis 3,Retinitis Pigmentosa 1,Retinitis Pigmentosa 9,Retinitis Pigmentosa 10,Leber Congenital Amaurosis 6,Leber Congenital Amaurosis 7,Leber Congenital Amaurosis 8,Leber Congenital Amaurosis 11,Leber Congenital Amaurosis 15,Leber Congenital Amaurosis 4,Usher Syndrome,Osteopetrosis, Autosomal Recessive 4,Osteopetrosis, Autosomal Recessive 6,Leber Congenital Amaurosis 16,Leber Congenital Amaurosis 10,Osteopetrosis, Autosomal Recessive 7,Leber Congenital Amaurosis 1,Leber Congenital Amaurosis 2,Osteopetrosis, Autosomal Recessive 1,Joubert Syndrome 1,Osteopetrosis, Autosomal Recessive 5

Bartter Disease,Arteriovenous Malformations Of The Brain,Spastic Paraplegia 45, Autosomal Recessive,Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia,Intracranial Aneurysm,Disease Of Mental Health,Hypomagnesemia 6, Renal,Schizophrenia,Urofacial Syndrome 1,Hypomagnesemia, Seizures, And Mental Retardation 1,Primary Hypomagnesemia

Trichuriasis,Malignant Essential Hypertension