Mondo Disease Ontology
201 terms(s) returned
| Term Type: | Record: 101 to 150 of 201 Records | Page: 3 of 5, First Previous Next Last | Show Records Per Page |
- 16p11 (Human)
- 16p11.2 (Human)
- 16p11.2-p12.2 (Human)
- 16p11.2p12.2 microduplication syndrome
- 16p12 (Human)
- 16p12.1 (Human)
- 16p12.1-p12.3 (Human)
- 16p12.1p12.3 triplication syndrome
- 16p12.2-p11.2 (Human)
- 16p13 (Human)
- 16p13.1 (Human)
- 16p13.11 (Human)
- 16p13.11 microdeletion syndrome
- 16p13.11 microduplication syndrome
- 16p13.2 (Human)
- 16p13.3 (Human)
- 16q (Human)
- 16q2 (Human)
- 16q22 (Human)
- 16q24 (Human)
- 16q24.1 (Human)
- 16q24.1 microdeletion syndrome
- 16q24.3 (Human)
- 16q24.3 microdeletion syndrome
- 17,20-lyase deficiency, isolated
- 17-alpha-hydroxylase/17,20-lyase deficiency, combined complete
- 17-alpha-hydroxylase/17,20-lyase deficiency, combined partial
- 17-beta-hydroxysteroid dehydrogenase (NADP+) activity
- 17-year-old stage
- 17p (Human)
- 17p1 (Human)
- 17p13 (Human)
- 17p13.1 (Human)
- 17p13.3 (Human)
- 17q (Human)
- 17q1 (Human)
- 17q11 (Human)
- 17q11.2 (Human)
- 17q11.2 microduplication syndrome
- 17q12 (Human)
- 17q2 (Human)
- 17q21 (Human)
- 17q21.3 (Human)
- 17q21.31 (Human)
- 17q23.1-q23.2 (Human)
- 17q24 (Human)
- 17q24.2 (Human)
- 17q24.2 microdeletion syndrome
- 18-oxo steroid
- 18-year-old stage
