Mondo Disease Ontology
109 terms(s) returned
| Term Type: Class | Record: 1 to 50 of 109 Records | Page: 1 of 3, First Previous Next Last | Show Records Per Page |
- (2R)-2-hydroxy monocarboxylic acid
- (2R)-2-hydroxy monocarboxylic acid anion
- (2R,3S)-2-aminooctadec-4-ene-1,3-diol
- (2S)-2-hydroxy monocarboxylic acid
- (2S)-2-hydroxy monocarboxylic acid anion
- 2-3 finger cutaneous syndactyly
- 2-3 toe syndactyly
- 2-4 finger cutaneous syndactyly
- 2-4 toe syndactyly
- 2-4 year-old child stage
- 2-5 toe syndactyly
- 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-hydroxy monocarboxylic acid
- 2-hydroxyethyl methacrylate sensitization
- 2-hydroxyglutaric aciduria
- 2-hydroxypropanoic acid
- 2-methylacetoacetyl CoA thiolase deficiency
- 2-methylbutyryl-CoA dehydrogenase deficiency
- 2-year-old stage
- 20-oxo steroid
- 20-year-old 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 stage
- 21q (Human)
- 21q22.11-q22.12 (Human)
- 21q22.11q22.12 microdeletion syndrome
- 21q22.13-q22.2 (Human)
