Select item 482735 Hemorrhage, intracerebral, susceptibility to Stroke, hemorrhagic, susceptibility to Select item 7467 Deficiency of alpha-mannosidase Alpha mannosidase B deficiency Alpha-Mannosidosis Lysosomal alpha-D-mannosidase deficiency Mannosidosis, alpha B lysosomal Select item 78691 3-methylcrotonyl-CoA carboxylase 1 deficiency 3 Alpha methylcrotonylglycinuria 1 MCC 1 deficiency MCCC1-Related 3-Methylcrotonyl-CoA Carboxylase Deficiency MCCD TYPE 1 METHYLCROTONYLGLYCINURIA TYPE I Select item 87542 Familial cancer of breast Breast cancer, familial Hereditary breast cancer Select item 41523 Type 2 diabetes mellitus DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST Diabetes mellitus, noninsulin-dependent, late onset KCNJ11-Related Susceptibility to Noninsulin-Dependent Diabetes Mellitus Type II diabetes mellitus Select item 461518 Smoking as a quantitative trait locus 3 Select item 9730 Acute myeloid leukemia AML adult Acute granulocytic leukemia Acute myelogenous leukemia Acute myeloid leukemia, adult Acute non-lymphocytic leukemia Familial Acute Myelocytic Leukemia Leukemia, acute myelogenous, somatic Leukemia, acute myeloid, somatic Select item 75696 Multiple acyl-CoA dehydrogenase deficiency Ethylmalonic-adipicaciduria GA 2 GA II Glutaric acidemia type 2 Glutaric acidemia type II Glutaric aciduria, type 2 Select item 1434 alpha Thalassemia A-Thalassemia Alpha thalassemia spectrum Select item 347898 3-methylcrotonyl-CoA carboxylase 2 deficiency 3 alpha methylcrotonyl-CoA carboxylase 2 deficiency 3 alpha methylcrotonylglycinuria 2 MCC 2 deficiency MCCC2-Related 3-Methylcrotonyl-CoA Carboxylase Deficiency METHYLCROTONYLGLYCINURIA, TYPE II Methylcrotonylglycinuria type 2 Select item 75694 Propionic acidemia Glycinemia, ketotic Hyperglycinemia with ketoacidosis and leukopenia Ketotic hyperglycinemia Select item 11713 Tay-Sachs disease GM2 gangliosidosis, type 1 HexA deficiency Hexosaminidase A Deficiency Hexosaminidase alpha-subunit deficiency (variant B) Sphingolipidosis, Tay-Sachs Select item 83428 Colorectal cancer Colorectal cancer, somatic Malignant Colorectal Neoplasm Select item 82790 Ehlers-Danlos syndrome, type 4 Ehlers Danlos syndrome, Sack-Barabas type Ehlers Danlos syndrome, arterial type Ehlers Danlos syndrome, ecchymotic type Ehlers-Danlos Syndrome Type IV Ehlers-Danlos syndrome vascular type Select item 9799 Osteogenesis imperfecta type I Classic Non-deforming Osteogenesis Imperfecta with Blue Sclerae Lobstein disease Lobstein's Disease OI type 1 OI type 1A OI, TYPE I Osteogenesis imperfecta tarda Osteogenesis imperfecta type 1 Osteogenesis imperfecta type 1 with dentinogenesis imperfecta Osteogenesis imperfecta type 1A Osteogenesis imperfecta with blue sclerae Osteogenesis imperfecta with opalescent teeth Select item 810955 Stickler syndrome type 1 Arthroophthalmopathy, hereditary progressive COL2A1-Associated Stickler Syndrome COL2A1-Related Stickler Syndrome Stickler syndrome, membranous vitreous type Stickler syndrome, vitreous type 1 Select item 69164 McCune-Albright syndrome Albright syndrome Albright's Syndrome Albright's disease McCune-Albright syndrome, somatic, mosaic Select item 1648433 X-linked Alport syndrome Alport Syndrome and Thin Basement Membrane Nephropathy Alport syndrome 1, X-linked recessive NEPHROPATHY AND DEAFNESS, X-LINKED Select item 463618 Parkinson disease, late-onset Hereditary late onset Parkinson disease PARKINSON DISEASE, LATE-ONSET, SUSCEPTIBILITY TO Parkinson disease, susceptibility to Parkinson's disease Susceptibility to Parkinson's Disease Select item 44264 Gastric cancer Malignant tumor of stomach Stomach cancer 
