Mondo Disease Ontology
36143 terms(s) returned
| Term Type: | Record: 1 to 50 of 36143 Records | Page: 1 of 723, First Previous Next Last | Show Records Per Page |
- 10p13-p14 deletion syndrome
- 10p15 microdeletion syndrome
- 10q22.3q23.3 microduplication syndrome
- 11p15.4 microduplication syndrome
- 11q22.2q22.3 microdeletion syndrome
- 12p12.1 microdeletion syndrome
- 12q14 microdeletion syndrome
- 12q15q21.1 microdeletion syndrome
- 13q12.3 microdeletion syndrome
- 14q11.2 microduplication syndrome
- 14q12 microdeletion syndrome
- 14q24.1q24.3 microdeletion syndrome
- 14q32 duplication syndrome
- 15q overgrowth syndrome
- 15q11q13 microduplication syndrome
- 15q14 microdeletion syndrome
- 16p11.2p12.2 microduplication syndrome
- 16p12.1p12.3 triplication 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
- 17q24.2 microdeletion syndrome
- 19p13.12 microdeletion syndrome
- 19p13.3 microduplication syndrome
- 1p21.3 microdeletion syndrome
- 1p35.2 microdeletion syndrome
- 1q44 microdeletion syndrome
- 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
- 2p25.3 microduplication syndrome
- 2q13 microdeletion syndrome
