Mondo Disease Ontology
57016 terms(s) returned
| Term Type: | Record: 301 to 350 of 57016 Records | Page: 7 of 1141, First Previous Next Last | Show Records Per Page |
- 2q2 (Human)
- 2q22 (Human)
- 2q23 (Human)
- 2q23.1 (Human)
- 2q23.1 microdeletion syndrome
- 2q23.1 microduplication syndrome
- 2q24 (Human)
- 2q24 microdeletion syndrome
- 2q3 (Human)
- 2q31 (Human)
- 2q31.1 (Human)
- 2q31.1 microdeletion syndrome
- 2q31.2 (Human)
- 2q32-q33 (Human)
- 2q33 (Human)
- 2q33.1 (Human)
- 2q33.1 microdeletion syndrome
- 2q35 (Human)
- 2q37 (Human)
- 2q37 microdeletion syndrome
- 3-4 finger osseus syndactyly
- 3-4 toe syndactyly
- 3-5 finger syndactyly
- 3-5 toe syndactyly
- 3-D extent
- 3-D shape
- 3-M syndrome
- 3-beta-hydroxysteroid dehydrogenase (NAD+)/C4-decarboxylase activity
- 3-beta-hydroxysteroid dehydrogenase [NAD(P)+]/C4-decarboxylase activity
- 3-hydroxy steroid
- 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 1 deficiency
- 3-methylcrotonyl-CoA carboxylase 2 deficiency
- 3-methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria
- 3-methylglutaconic aciduria type 1
- 3-methylglutaconic aciduria type 3
- 3-methylglutaconic aciduria type 4
- 3-methylglutaconic aciduria type 5
- 3-methylglutaconic aciduria type 8
- 3-methylglutaconic aciduria type 9
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- 3-methylglutaconic aciduria, type VIIA
- 3-methylglutaconic aciduria, type VIIB
- 3-oxo steroid
- 3-oxo-Delta(4) steroid
