Mondo Disease Ontology
57106 terms(s) returned
| Term Type: | Record: 551 to 600 of 57106 Records | Page: 12 of 1143, First Previous Next Last | Show Records Per Page |
- 8p11.2 (Human)
- 8p11.2 deletion syndrome
- 8p2 (Human)
- 8p23 (Human)
- 8p23.1 (Human)
- 8p23.1 duplication syndrome
- 8p23.1 microdeletion syndrome
- 8q (Human)
- 8q1 (Human)
- 8q12 (Human)
- 8q12 microduplication syndrome
- 8q12.1-q21.2 (Human)
- 8q2 (Human)
- 8q21 (Human)
- 8q21.1 (Human)
- 8q21.11 (Human)
- 8q22 (Human)
- 8q22.1 (Human)
- 8q22.1 microdeletion syndrome
- 8q24 (Human)
- 8q24.3 (Human)
- 8q24.3 microdeletion syndrome
- 9+2 motile cilium
- 9-year-old stage
- 9p (Human)
- 9p1 (Human)
- 9p13 (Human)
- 9p13 microdeletion syndrome
- 9q (Human)
- 9q2 (Human)
- 9q21 (Human)
- 9q21.1 (Human)
- 9q21.13 (Human)
- 9q21.13 microdeletion syndrome
- 9q22 (Human)
- 9q22.3 (Human)
- 9q3 (Human)
- 9q31.1-q31.3 (Human)
- 9q31.1q31.3 microdeletion syndrome
- 9q33.3-q34.11 (Human)
- 9q33.3q34.11 microdeletion syndrome
- 9q34 (Human)
- A axonemal microtubule
- A synonym that is historic and discouraged
- A synonym that is recorded for consistency with another source but is a misspelling
- A synonym that is used for non-human animal variants of a disease
- A20 haploinsufficiency
- A2M
- A4GALT
- A4GALT-congenital disorder of glycosylation
