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 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 137902 Autosomal dominant optic atrophy classic form Kjer-type optic atrophy Optic Atrophy Type 1 Optic atrophy, juvenile Select item 7517 Medulloblastoma MEDULLOBLASTOMA PREDISPOSITION SYNDROME Medulloblastoma, SUFU-Related Medulloblastoma, somatic Select item 373469 Multiple endocrine neoplasia type 4 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV 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 87450 Oculocutaneous albinism type 3 ALBINISM III Albinism 3 Albinism, oculocutaneous, type III Rufous OCA Rufous albinism Rufous oculocutaneous albinism Xanthism Select item 1643910 Tyrosinase-negative oculocutaneous albinism Albinism, oculocutaneous, type IA Oculocutaneous albinism type 1A Select item 199598 UDPglucose-4-epimerase deficiency Epimerase Deficiency Galactosemia GALACTOSEMIA III Galactose epimerase deficiency Galactosemia 3 UDP-Galactose-4-epimerase deficiency UDPglucose 4-Epimerase Deficiency Disease Select item 346653 Hereditary angioedema type 3 ANGIONEUROTIC EDEMA, HEREDITARY, WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION ESTROGEN-RELATED HAE ESTROGEN-SENSITIVE HAE HAE WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION Hereditary angioedema, type III Select item 357420 Polysyndactyly 4 Polysyndactyly uncomplicated Preaxial Polydactyly Type IV Preaxial polydactyly 4 Select item 2212 Bernard Soulier syndrome BLEEDING DISORDER, PLATELET-TYPE, 1 GLYCOPROTEIN Ib, PLATELET, DEFICIENCY OF Giant platelet disease Giant platelet syndrome Hemorrhagiparous thrombocytic dystrophy PLATELET GLYCOPROTEIN Ib DEFICIENCY Platelet glycoprotein 1b, deficiency of Von Willebrand factor receptor deficiency Select item 339667 Nephronophthisis 4 NEPHRONOPHTHISIS 4, JUVENILE Select item 349786 Waardenburg syndrome type 2A WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM Waardenburg Syndrome Type IIA Select item 6642 Glycogen storage disease, type IV Amylopectinosis Andersen disease Brancher deficiency Cirrhosis, familial, with deposition of abnormal glycogen GBE1 DEFICIENCY GLYCOGENOSIS IV GSD 4 GSD IV Glycogen branching enzyme deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Glycogen storage disease type 4 Glycogenosis 4 Select item 2980 Charcot-Marie-Tooth disease Charcot-Marie-Tooth Neuropathy Charcot-Marie-Tooth hereditary neuropathy Select item 372151 Congenital malabsorptive diarrhea 4 Select item 452446 3 beta-Hydroxysteroid dehydrogenase deficiency 3-beta-HSD deficiency 3-beta-Hydroxysteroid Dehydrogenase-Deficient Congenital Adrenal Hyperplasia 3b-hydroxysteroid dehydrogenase deficiency ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY Adrenal hyperplasia 2 Adrenal hyperplasia II Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency HSD3B deficiency Type II 3-beta-hydroxysteroid dehydrogenase deficiency 
