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Boli A-Z Acromegaly Acute Lymphocytic Leukemia Acute Promyelocytic Leukemia Adenocarcinoma Aging Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome and Thin Basement Membrane Nephropathy Alport Syndrome, Autosomal Dominant Alport Syndrome, Autosomal Recessive Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm Angiokeratoma of Fordyce Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arteriolosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Septal Defect 3 Autosomal Dominant Intermediate Charcot-Marie-Tooth Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 C1q Nephropathy Calciphylaxis Charcot-Marie-Tooth Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Kidney Failure Chronic Progressive External Ophthalmoplegia Churg-Strauss Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Corneal Dystrophy, Meesmann Crescentic Glomerulonephritis Danubian Endemic Familial Nephropathy Demyelinating Polyneuropathy Denys-Drash Syndrome Desquamative Interstitial Pneumonia Diabetes Mellitus Diffuse Mesangial Sclerosis Donnai-Barrow Syndrome Embryonal Rhabdomyosarcoma Encephalitis Encephalomyopathy Encephalopathy Endotheliitis End Stage Renal Failure Epidermolysis Bullosa Essential Thrombocythemia Familial Glucocorticoid Deficiency Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes Familial Nephrotic Syndrome Familial Partial Lipodystrophy Fanconi Syndrome Focal Segmental Glomerulosclerosis 1 Frasier Syndrome Galloway-Mowat Syndrome Gitelman Syndrome Glomerulonephritis Goodpasture Syndrome Graft-Versus-Host Disease Growth Hormone Deficiency Guillain-Barre Syndrome Hematuria, Benign Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Wilms' Tumor Herpes Simplex Homozygous Familial Hypercholesterolemia Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanosis of Ito Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Iga Glomerulonephritis Interstitial Nephritis Juvenile Rheumatoid Arthritis Kartagener Syndrome Kidney Disease Kidney Hypertrophy Kimura Disease Lactic Acidosis Leiomyomatosis Leukemia Lipodystrophy Lipoid Nephrosis Lupus Erythematosus Lymphoma Macular Dystrophy, Corneal Malignant Hypertension Mantle Cell Lymphoma Marfan Syndrome Membranoproliferative Glomerulonephritis Membranous Nephropathy Mesangial Proliferative Glomerulonephritis Metaphyseal Chondrodysplasia, Schmid Type Metaphyseal Dysplasia, Spahr Type Microcephaly Microvascular Complications of Diabetes 3 Mitochondrial Encephalomyopathy Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Nail-Patella Syndrome Nephrocalcinosis Nephrosclerosis Nephrotic Syndrome Nephrotic Syndrome, Idiopathic, Steroid-Resistant Nephrotic Syndrome, Type 1 Neuritis Neurofibromatosis, Type Iv, of Riccardi Neuropathy Obesity-Hypoventilation Syndrome Optic Neuritis Phenylketonuria Pierson Syndrome Pituitary Hormone Deficiency, Combined, 2 Pneumonia Poems Syndrome Polycystic Kidney Disease Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polyneuropathy Polyradiculopathy Primary Biliary Cirrhosis Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Proliferative Glomerulonephritis Psoriasis Psoriasis 13 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sarcoidosis Purpura Renal Tubular Acidosis Renovascular Hypertension Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatoid Arthritis Riddle Syndrome Sarcoidosis 2 Sensorineural Hearing Loss Sickle Cell Anemia Sleep Apnea Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis Systemic Lupus Erythematosus Takayasu Arteritis Thrombocytopenia Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Tooth Disease Undifferentiated Pleomorphic Sarcoma Urinary System Disease Viral Encephalitis Wilms Tumor 5 Wilms Tumor 6