Mondo Disease Ontology
2425 terms(s) returned
| Term Type: | Record: 2401 to 2425 of 2425 Records | Page: 49 of 49, First Previous Next Last | Show Records Per Page |
- pyrimidine metabolism disease
- pyromania
- pyropoikilocytosis, hereditary
- pyruvate carboxylase deficiency disease
- pyruvate carboxylase deficiency, benign type
- pyruvate carboxylase deficiency, infantile form
- pyruvate carboxylase deficiency, severe neonatal type
- 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 deficiency
- pyruvate dehydrogenase deficiency, dog
- pyruvate dehydrogenase deficiency, non-human animal
- pyruvate dehydrogenase phosphatase deficiency
- pyruvate kinase deficiency of erythrocyte, dog
- pyruvate kinase deficiency of erythrocyte, domestic cat
- pyruvate kinase deficiency of erythrocyte, non-human animal
- pyruvate kinase deficiency of red cells
- pyruvate kinase hyperactivity
- pyruvate metabolism disorder
- pythiosis
- pythiosis, non-human animal
- pyuria
