Mondo Disease Ontology
94 terms(s) returned
| Term Type: Class | Record: 1 to 50 of 94 Records | Page: 1 of 2, First Previous Next Last | Show Records Per Page |
- (2R,3S)-2-aminooctadec-4-ene-1,3-diol
- 2-5 year-old child stage
- 2-D shape
- 2-aminoadipic 2-oxoadipic aciduria
- 2-aminooctadec-4-ene-1,3-diol
- 2-aminooctadecene-1,3-diol
- 2-carboxyethyl group
- 2-hydroxyethyl methacrylate sensitization
- 2-hydroxyglutaric aciduria
- 2-methylacetoacetyl CoA thiolase deficiency
- 2-methylbutyryl-CoA dehydrogenase deficiency
- 2-year-old human stage
- 20-oxo steroid
- 20-year-old human stage
- 20p (Human)
- 20p1 (Human)
- 20p12 (Human)
- 20p12.3 (Human)
- 20p12.3 microdeletion syndrome
- 20p13 (Human)
- 20p13 microdeletion syndrome
- 20q (Human)
- 20q1 (Human)
- 20q11 (Human)
- 20q11.2 (Human)
- 20q11.2 microdeletion syndrome
- 20q11.2 microduplication syndrome
- 20q13 (Human)
- 20q13.2-q13.3 (Human)
- 20q13.3 (Human)
- 20q13.33 (Human)
- 20q13.33 microdeletion syndrome
- 21-hydroxy steroid
- 21-year-old human stage
- 21q (Human)
- 21q22.11-q22.12 (Human)
- 21q22.11q22.12 microdeletion syndrome
- 21q22.13-q22.2 (Human)
- 22-year-old human stage
- 22q (Human)
- 22q1 (Human)
- 22q11 (Human)
- 22q11.2 (Human)
- 22q11.2 deletion syndrome
- 22q13 (Human)
- 23-year-old human stage
- 24-year-old human stage
- 24G7 epitope
- 25-44 year-old human stage
- 25-year-old human stage
