Mitochondrial Encephalomyopathy,Familial Renal Papillary Carcinoma,Diabetic Macular Edema,Eosinophilic Variant Of Chromophobe Renal Cell Carcinoma,Leiomyosarcoma,Hereditary Renal Cell Carcinoma,Acth-Independent Macronodular Adrenal Hyperplasia,Dermis Tumor,Inherited Cancer-Predisposing Syndrome,Leiomyoma,Bizarre Leiomyoma,Kidney Cancer,Leiomyoma Cutis,Leiomyomatosis,Cystadenoma,Dartoic Leiomyoma,Fh Tumor Predisposition Syndrome,Myoma,Fumarate Hydratase Deficiency,Hereditary Paraganglioma-Pheochromocytoma Syndromes,Cutaneous Leiomyosarcoma,Gastric Leiomyoma,Polyhydramnios,Brain Cancer,Cystic Kidney Disease,Colon Leiomyoma,Hemolytic Anemia,Pheochromocytoma,Encephalopathy,Cardiomyopathy, Dilated, 1gg,Renal Cell Carcinoma, Papillary, 1,Birt-Hogg-Dube Syndrome,Reproductive Organ Benign Neoplasm,Tumor Predisposition Syndrome,Paraganglioma,Fumarase Deficiency,Paraganglioma And Gastric Stromal Sarcoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Multiple Enchondromatosis, Maffucci Type,Cell Type Benign Neoplasm,Endocrine Organ Benign Neoplasm,Uterine Benign Neoplasm,Leiomyoma, Uterine,Hereditary Leiomyomatosis And Renal Cell Cancer,Persistent Generalized Lymphadenopathy,Oncocytoma,3-Methylglutaconic Aciduria, Type Iii,D-2-Hydroxyglutaric Aciduria 1

Citrullinemia, Classic,Amino Acid Metabolic Disorder,Urea Cycle Disorder,Peroxisome Biogenesis Disorder 1b,Lysinuric Protein Intolerance,Tyrosinemia, Type I,Citrullinemia, Type Ii, Adult-Onset,Bardet-Biedl Syndrome 2,Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome,Pyrimidine Metabolic Disorder,Fumarase Deficiency,Maple Syrup Urine Disease,Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To,Argininemia,Argininosuccinic Aciduria,Orotic Aciduria