| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013421 |
BXGD000837 |
Dystonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0018522 |
BXGD001198 |
Hallermann's Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0018523 |
BXGD001199 |
Hallervorden-Spatz Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0038160 |
BXGD002734 |
Staphylococcal Infections |
Infections |
| C0202098 |
BXGD004070 |
Insulin measurement |
|
| C0242422 |
BXGD005163 |
Parkinsonian Disorders |
Nervous System Diseases |
| C0270724 |
BXGD006092 |
Infantile Neuroaxonal Dystrophy |
Nervous System Diseases |
| C0337438 |
BXGD007159 |
Glucose measurement |
|
| C0344482 |
BXGD007678 |
Hypoplasia of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0346648 |
BXGD007833 |
Malignant tumor of exocrine pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0393593 |
BXGD008103 |
Dystonia Disorders |
Nervous System Diseases |
| C0495706 |
BXGD009038 |
elevated blood glucose level |
|
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0596887 |
BXGD009648 |
mathematical ability |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1837657 |
BXGD014256 |
Spondyloepiphyseal dysplasia, Omani type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1853578 |
BXGD015346 |
Neuroferritinopathy |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1858479 |
BXGD015798 |
Spastic paraplegia 11, autosomal recessive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C2931356 |
BXGD018007 |
Spastic paraplegia type 5A, recessive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C2931845 |
BXGD018076 |
Neurodegeneration with brain iron accumulation (NBIA) |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C3550973 |
BXGD019143 |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |