Mondo Disease Ontology
4286 terms(s) returned
| Term Type: Class | Record: 4251 to 4286 of 4286 Records | Page: 86 of 86, First Previous Next Last | Show Records Per Page |
- pyridoxine
- pyridoxine deficiency anemia
- pyridoxine metabolic process
- pyridoxine-dependent epilepsy
- pyridoxine-dependent epilepsy caused by ALDH7A1 mutant
- pyridoxine-responsive sideroblastic anemia
- pyriform sinus cancer
- pyrimidine metabolism disease
- pyrimidine nucleobase metabolic process
- pyrimidine-containing compound metabolic process
- pyrimidines
- pyrimidone
- pyromania
- pyrophosphatase activity
- pyropoikilocytosis, hereditary
- pyruvate biosynthetic process
- pyruvate carboxylase deficiency disease
- pyruvate carboxylase deficiency, benign type
- pyruvate carboxylase deficiency, infantile form
- pyruvate carboxylase deficiency, severe neonatal type
- pyruvate decarboxylase activity
- pyruvate dehydrogenase E1-alpha deficiency
- pyruvate dehydrogenase E1-beta deficiency
- pyruvate dehydrogenase E2 deficiency
- pyruvate dehydrogenase E3 deficiency
- pyruvate dehydrogenase E3-binding protein deficiency
- pyruvate dehydrogenase complex
- pyruvate dehydrogenase deficiency
- pyruvate dehydrogenase phosphatase deficiency
- pyruvate kinase activity
- pyruvate kinase deficiency of red cells
- pyruvate kinase hyperactivity
- pyruvate metabolic process
- pyruvate metabolism disorder
- pythiosis
- pyuria
