Congenital Mesoblastic Nephroma

Skin Melanoma,Endometrial Cancer,Bartholin'S Gland Adenocarcinoma,Cowden Syndrome,Melanoma,Cowden Syndrome 1,Bardet-Biedl Syndrome,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Transient Neonatal Thrombocytopenia,Nevus, Epidermal,Glioma,Hemimegalencephaly,Pneumococcal Meningitis,Capillary Hemangioma,Polymicrogyria,Ovarian Cancer,Breast Cancer,Glioblastoma,Colorectal Cancer,Colon Leiomyoma,Hepatocellular Carcinoma,Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome,Microcephaly,Hydrocephalus,Megalencephaly,Thymoma,Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1,Senior-Loken Syndrome 7,Transient Neonatal Neutropenia,Skin Carcinoma,Polydactyly,Prostate Cancer,Disease Of Mental Health,Corneal Dystrophy, Fleck,Microcephaly With Simplified Gyral Pattern,Proteus Syndrome,Hypomelanosis Of Ito,Retinal Aplasia,Albinism, Ocular, With Late-Onset Sensorineural Deafness,Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2,Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations,Bardet-Biedl Syndrome 16,Macrocephaly/Autism Syndrome,Periventricular Nodular Heterotopia,Tuberous Sclerosis 1,Meningioma, Familial,Melanoma, Cutaneous Malignant 1,Autosomal Dominant Non-Syndromic Intellectual Disability 19,Lung Cancer,Pancreatic Cancer

Aleutian Mink Disease,Nephronophthisis 3

Cholecystolithiasis

Rhizomelic Chondrodysplasia Punctata, Type 3

Cleft Lip,Cleft Lip With Or Without Cleft Palate,Blepharocheilodontic Syndrome 1

Wernicke-Korsakoff Syndrome,Thiamine Deficiency Disease

Hereditary Spastic Paraplegia,Charcot-Marie-Tooth Disease,Interstitial Lung And Liver Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2u

Vertebral Artery Insufficiency,Robinow Syndrome, Autosomal Dominant 2,Finger Agnosia,Robinow Syndrome

Pneumocystosis,X-Linked Recessive Disease,Lymphopenia,Conjunctivitis,Richter'S Syndrome,Macroglobulinemia,Pyoderma,Cll/Sll,Mast-Cell Leukemia,Polyarticular Juvenile Idiopathic Arthritis,Spherocytosis, Type 5,Ecthyma,B Cell Deficiency,Lung Large Cell Carcinoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Neutropenia,Agammaglobulinemia 1, Autosomal Recessive,Plasma Protein Metabolism Disease,Isolated Agammaglobulinemia,Poliomyelitis,Leukemia, Acute Myeloid,Growth Hormone Deficiency,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Bacterial Infectious Disease,Breast Cancer,Central Nervous System Hematologic Cancer,Congenital Hypogammaglobulinemia,Immunodeficiency 14,Panniculitis,Immunodeficiency 33,Lymphoma, Non-Hodgkin, Familial,Baylisascariasis,Agammaglobulinemia, X-Linked,Paralytic Poliomyelitis,Immune Deficiency Disease,Myelodysplastic Syndrome,Immunoglobulin A Deficiency 1,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Diffuse Large B-Cell Lymphoma,Mantle Cell Lymphoma,Lymphoplasmacytic Lymphoma,Marginal Zone B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Williams-Beuren Syndrome,Combined Oxidative Phosphorylation Deficiency 9,Mohr-Tranebjaerg Syndrome,Cd40 Ligand Deficiency,Isolated Growth Hormone Deficiency, Type Iii, With Agammaglobulinemia,Immunodeficiency 45,Immunodeficiency With Hyper-Igm, Type 1,Leukemia, Chronic Lymphocytic,Myeloma, Multiple,Isolated Growth Hormone Deficiency,Isolated Growth Hormone Deficiency Type Iii,Waldenstroem'S Macroglobulinemia

Excessive Tearing

Familial Vesicoureteral Reflux,Vesicoureteral Reflux 1,Cartilage Cancer

Dilated Cardiomyopathy,Vici Syndrome,Left Ventricular Noncompaction

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

Primary Mediastinal B-Cell Lymphoma,Cold Urticaria,Autoinflammation, Antibody Deficiency, And Immune Dysregulation,B Cell Deficiency,B-Cell Lymphoma,Familial Cold Autoinflammatory Syndrome,Autoinflammatory Syndrome,Trichohepatoenteric Syndrome 1,Urticaria,Thrombocytopenia,Agammaglobulinemia, X-Linked,Bleeding Disorder, Platelet-Type, 11,Gray Platelet Syndrome,Familial Cold Autoinflammatory Syndrome 3,Combined Oxidative Phosphorylation Deficiency 9,Leukemia, Chronic Lymphocytic,Frontotemporal Dementia

Retinitis Pigmentosa,Nystagmus 7, Congenital, Autosomal Dominant,Cowden Syndrome,Cowden Syndrome 1,Rasopathy,Myopathy, Centronuclear, 1,Leukocyte Adhesion Deficiency, Type Iii,Skin Granular Cell Tumor,Nystagmus 2, Congenital, Autosomal Dominant,Agammaglobulinemia,Osteopetrosis,Charcot-Marie-Tooth Disease,Leukocyte Adhesion Deficiency, Type I,Developmental And Epileptic Encephalopathy 5,Deficiency Anemia,Immunodeficiency 14,Centronuclear Myopathy,Disease Of Mental Health,Deafness, Autosomal Dominant 58,Proteus Syndrome,Neuropathy, Hereditary Sensory, Type Id,Congenital Myasthenic Syndrome,Agammaglobulinemia, X-Linked,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Charcot-Marie-Tooth Disease Intermediate Type,Ritscher-Schinzel Syndrome 2,Wiskott-Aldrich Syndrome,Charcot-Marie-Tooth Disease, Dominant Intermediate B,Nystagmus 4, Congenital, Autosomal Dominant,Aarskog-Scott Syndrome,Lowe Oculocerebrorenal Syndrome,Spinocerebellar Ataxia 5,Palmoplantar Keratoderma, Bothnian Type,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease,Scott Syndrome

Autosomal Dominant Polycystic Kidney Disease,Cystic Kidney Disease,Prostate Cancer,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease

Chronic Myelomonocytic Leukemia