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 414431 Glioma susceptibility 2 Select item 382625 Breast-ovarian cancer, familial, susceptibility to, 2 BRCA2 Hereditary Breast and Ovarian Cancer Breast-ovarian cancer, familial 2 Select item 138111 PMM2-congenital disorder of glycosylation CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE Ia CDG 1A CDG Ia Carbohydrate-deficient glycoprotein syndrome type 1A Carbohydrate-deficient glycoprotein syndrome type 1A (formerly) Congenital disorder of glycosylation type 1A Congenital disorder of glycosylation, type Ia Jaeken syndrome PMM2-CDG PMM2-CDG (CDG-Ia) Phosphomannomutase 2 deficiency Select item 45811 Familial Mediterranean fever Benign paroxysmal peritonitis Familial Mediterranean Fever Type 1 Familial Mediterranean Fever Type 2 POLYSEROSITIS, FAMILIAL PAROXYSMAL POLYSEROSITIS, RECURRENT Periodic disease Periodic peritonitis Select item 18014 Neurofibromatosis, type 2 Acoustic neurinoma bilateral Acoustic schwannomas bilateral Bilateral acoustic neurofibromatosis NF 2 Neurofibromatosis central type Neurofibromatosis type II SCHWANNOMATOSIS, VESTIBULAR Select item 155704 Spinocerebellar ataxia type 2 CEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS OLIVOPONTOCEREBELLAR ATROPHY II Olivopontocerebellar atrophy 2 Olivopontocerebellar atrophy Holguin type SCA 2 SPINOCEREBELLAR ATROPHY II Spinocerebellar ataxia Cuban type Spinocerebellar ataxia with slow eye movements Spinocerebellar atrophy 2 Wadia Swami syndrome Select item 331891 Melanoma, cutaneous malignant, susceptibility to, 2 CDKN2A-Related Cutaneous Malignant Melanoma Cutaneous malignant melanoma 2 Select item 325025 Dyslexia, susceptibility to, 2 Dyslexia 2 READING DISABILITY, SPECIFIC, 2 Select item 78652 Gaucher disease type II Acute neuronopathic Gaucher's disease GD 2 GD II Gaucher Disease Type 2 (Acute) Gaucher disease type 2 Gaucher disease, acute neuronopathic type Gaucher disease, infantile cerebral Select item 381193 Atrioventricular septal defect, susceptibility to, 2 Atrioventricular septal defect 2 Select item 414167 Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly AHUS, SUSCEPTIBILITY TO, 2 Atypical hemolytic-uremic syndrome 2 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2 Select item 481726 Transferrin serum level quantitative trait locus 2 Select item 369417 Colorectal cancer, susceptibility to, 2 COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 8q24 CRCS2 Colorectal cancer 2 Select item 314039 Episodic ataxia type 2 Acetazolamide-responsive episodic ataxia syndrome Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia Ataxia, familial, paroxysmal Cerebellar ataxia, paroxysmal, Acetazolamide-responsive Cerebellopathy, hereditary paroxysmal Episodic ataxia with nystagmus Nystagmus-associated episodic ataxia 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 224736 von Willebrand disease type 2 VON WILLEBRAND DISEASE, TYPE 2A/IIE VON WILLEBRAND DISEASE, TYPE 2CB VON WILLEBRAND DISEASE, TYPE II VWD, TYPE 2 Select item 340052 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 Ataxia with Oculomotor Apraxia Ataxia with Oculomotor Apraxia 2 Ataxia-ocular apraxia-2 Ataxia-oculomotor apraxia 2 Select item 79381 Chondrodysplasia punctata 2 X-linked dominant CONRADI-HUNERMANN-HAPPLE SYNDROME Chondrodysplasia punctata, X-linked dominant Conrad Hunermann Happle syndrome Happle syndrome Hunermann-Conradi Syndrome 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 
