Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease

Melanoma,Leukemia, Chronic Myeloid,Latent Syphilis,Sjogren-Larsson Syndrome,Leukemia,Myeloid Leukemia,Sarcoma,Ewing Sarcoma Of Bone,Neurofibrosarcoma,Acute Promyelocytic Leukemia,Miller-Dieker Lissencephaly Syndrome,Myopathy, Centronuclear, 2

Leukemia, Chronic Myeloid,Tinea Favosa,Renal Pelvis Adenocarcinoma,Leukemia, Acute Lymphoblastic,Human Immunodeficiency Virus Type 1,Co-Trimoxazole Allergy,Immune Deficiency Disease

Glycogen Storage Disease Ixa,Glycogen Storage Disease Ixc,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency,Glycogen Storage Disease Ia,Glycogen Storage Disease, Type Ixd,Glycogen Storage Disease Ix,Glycogen Storage Disease Ixb

Heart Disease,Alzheimer Disease,Myocardial Infarction,Exudative Vitreoretinopathy 5,Colorectal Cancer,Disease Of Mental Health,Hypertension, Essential

Large Cell Carcinoma,Lung Large Cell Carcinoma,Cerebral Artery Occlusion,Adenocarcinoma,Breast Cancer,Beriberi,Parkinson Disease, Late-Onset,Colorectal Cancer,Thiamine Deficiency Disease,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Wet Beriberi

Cardiomyopathy, Familial Restrictive, 2,Deafness, Autosomal Recessive 17,Deafness, Autosomal Recessive 14,Cardiomyopathy, Familial Restrictive, 3

Mitochondrial Encephalomyopathy,Nephrotic Syndrome,Pathologic Nystagmus,Chronic Progressive External Ophthalmoplegia,Leigh Syndrome With Nephrotic Syndrome,Cerebellar Disease,Mitochondrial Disorders,Spinocerebellar Ataxia, Autosomal Recessive 14,Cardiofaciocutaneous Syndrome 1,Multiple Acyl-Coa Dehydrogenase Deficiency,Aceruloplasminemia,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Spinocerebellar Ataxia, Autosomal Recessive 8,Coenzyme Q10 Deficiency, Primary, 4,Coenzyme Q10 Deficiency, Primary, 7,Coenzyme Q10 Deficiency Disease,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Joubert Syndrome 17,Coenzyme Q10 Deficiency, Primary, 6,Coenzyme Q10 Deficiency, Primary, 5,Spastic Paraplegia 7, Autosomal Recessive,Coenzyme Q10 Deficiency, Primary, 1,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Mitochondrial Complex I Deficiency, Nuclear Type 1,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Leigh Syndrome

T-Cell Lymphoblastic Leukemia/Lymphoma,Nik Deficiency,Trichohepatoenteric Syndrome 1,Pancreatic Adenosquamous Carcinoma,Pancreatic Ductal Adenocarcinoma,Immunodeficiency 50