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 400313 Hypercholesterolemia, familial, 4 Familial Hypercholesterolemia, Autosomal Recessive HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE, 1 HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE, 2 Hypercholesterolemia, autosomal recessive Select item 152875 Hypercholesterolemia, familial, 1 Fredrickson type IIa hyperlipoproteinemia HYPER-LOW-DENSITY-LIPOPROTEINEMIA HYPERCHOLESTEROLEMIA, FAMILIAL, MODIFIER OF HYPERCHOLESTEROLEMIC XANTHOMATOSIS, FAMILIAL Hyper-beta-lipoproteinemia Hyperlipoproteinemia Type II Hyperlipoproteinemia Type IIa Hyperlipoproteinemia type 2 LDL RECEPTOR DISORDER LDLR-Related Familial Hypercholesterolemia, Autosomal Dominant 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 48574 Schizophrenia Select item 383691 Severe early-childhood-onset retinal dystrophy ABCA4-Related Stargardt Disease 1 CNGB3-Related Stargardt Disease 1 Juvenile onset macular degeneration MACULAR DYSTROPHY WITH FLECKS, TYPE 1 STGD Stargardt disease 1 Stargardt macular dystrophy Select item 6915 Hereditary insensitivity to pain with anhidrosis FAMILIAL DYSAUTONOMIA, TYPE II Familial dysautonomia, type 2 HSAN 4 HSAN Type IV Hereditary Sensory and Autonomic Neuropathy Type IV Hereditary sensory and autonomic neuropathy 4 Insensitivity to pain, congenital, with anhidrosis Neuropathy, congenital sensory, with anhidrosis Select item 373469 Multiple endocrine neoplasia type 4 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV Select item 7517 Medulloblastoma MEDULLOBLASTOMA PREDISPOSITION SYNDROME Medulloblastoma, SUFU-Related Medulloblastoma, somatic Select item 332156 Susceptibility to HIV infection HIV-1, SUSCEPTIBILITY TO HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RESISTANCE TO Human immunodeficiency virus type 1, susceptibility to Select item 1648386 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1 TREM2-Related Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy TYROBP-Related Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy Select item 1643910 Tyrosinase-negative oculocutaneous albinism Albinism, oculocutaneous, type IA Oculocutaneous albinism type 1A Select item 307153 Autism spectrum disorder Autism spectrum disorders Select item 5340 Glycogen storage disease, type II ACID ALPHA-GLUCOSIDASE DEFICIENCY Acid maltase deficiency disease Aglucosidase alfa Alpha-1,4-glucosidase deficiency Cardiomegalia glycogenica diffusa Deficiency of alpha-glucosidase Deficiency of lysosomal alpha-glucosidase GLYCOGENOSIS, GENERALIZED, CARDIAC FORM GSD II Glucosidase acid-1,4-alpha deficiency Glycogen Storage Disease Type II (Pompe Disease) Glycogen storage disease type 2 POMPE DISEASE Select item 349786 Waardenburg syndrome type 2A WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM Waardenburg Syndrome Type IIA Select item 904175 Thyroid cancer, nonmedullary, 2 THYROID CANCER, NONMEDULLARY, 2, SUSCEPTIBILITY TO THYROID CARCINOMA, FOLLICULAR Thyroid carcinoma, follicular, somatic Select item 318623 Wilms tumor 4 Select item 2980 Charcot-Marie-Tooth disease Charcot-Marie-Tooth Neuropathy Charcot-Marie-Tooth hereditary neuropathy Select item 414347 Familial juvenile hyperuricemic nephropathy type 2 EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 4 Select item 87450 Oculocutaneous albinism type 3 ALBINISM III Albinism 3 Albinism, oculocutaneous, type III Rufous OCA Rufous albinism Rufous oculocutaneous albinism Xanthism 
