Mondo Disease Ontology
57016 terms(s) returned
| Term Type: | Record: 201 to 250 of 57016 Records | Page: 5 of 1141, First Previous Next Last | Show Records Per Page |
- 1q44 microdeletion syndrome
- 1st arch mandibular component
- 1st arch mandibular endoderm
- 1st arch mandibular mesenchyme
- 1st arch mandibular mesenchyme from head mesenchyme
- 1st arch mandibular mesenchyme from neural crest
- 1st arch maxillary component
- 1st arch maxillary ectoderm
- 1st arch maxillary mesenchyme
- 1st arch maxillary mesenchyme from head mesenchyme
- 1st arch maxillary mesenchyme from neural crest
- 1st arch mesenchyme
- 1st arch mesenchyme from head mesenchyme
- 1st arch mesenchyme from neural crest
- 1st arch pharyngeal cleft
- 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)
