Mondo Disease Ontology
22 terms(s) returned
| Term Type: | Record: 1 to 22 of 22 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- 2-aminoadipic 2-oxoadipic aciduria
- 2-hydroxyethyl methacrylate sensitization
- 2-hydroxyglutaric aciduria
- 2-methylacetoacetyl CoA thiolase deficiency
- 2-methylbutyryl-CoA dehydrogenase deficiency
- 20p12.3 microdeletion syndrome
- 20p13 microdeletion syndrome
- 20q11.2 microdeletion syndrome
- 20q11.2 microduplication syndrome
- 20q13.33 microdeletion syndrome
- 21q22.11q22.12 microdeletion syndrome
- 22q-related schwannomatosis
- 22q11.2 deletion syndrome
- 2p13.2 microdeletion syndrome
- 2p21 microdeletion syndrome
- 2p21 microdeletion syndrome without cystinuria
- 2q23.1 microdeletion syndrome
- 2q23.1 microduplication syndrome
- 2q24 microdeletion syndrome
- 2q31.1 microdeletion syndrome
- 2q33.1 microdeletion syndrome
- 2q37 microdeletion syndrome
