Experimental Factor Ontology
12203 terms(s) returned
| Term Type: | Record: 1 to 50 of 12203 Records | Page: 1 of 245, First Previous Next Last | Show Records Per Page |
- 10q22.3q23.3 microduplication syndrome
- 11p15.4 microduplication syndrome
- 12p12.1 microdeletion syndrome
- 12q14 microdeletion syndrome
- 12q15q21.1 microdeletion syndrome
- 14q11.2 microduplication syndrome
- 14q12 microdeletion syndrome
- 14q24.1q24.3 microdeletion syndrome
- 15q overgrowth syndrome
- 15q11q13 microduplication syndrome
- 15q14 microdeletion syndrome
- 16p11.2p12.2 microduplication syndrome
- 16p13.11 microdeletion syndrome
- 16p13.11 microduplication syndrome
- 16q24.1 microdeletion syndrome
- 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
- 17q11.2 microduplication syndrome
- 19p13.12 microdeletion syndrome
- 19p13.3 microduplication syndrome
- 1p21.3 microdeletion syndrome
- 1q44 microdeletion syndrome
- 2-aminoadipic 2-oxoadipic aciduria
- 2-hydroxyglutaric aciduria
- 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
- 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
- 3-M syndrome
- 3-hydroxy-3-methylglutaric aciduria
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
- 3-hydroxyacyl-CoA dehydrogenase deficiency
- 3-hydroxyisobutyric aciduria
- 3-hydroxyisobutyryl-CoA hydrolase deficiency
- 3-methylcrotonyl-CoA carboxylase 2 deficiency
