Mondo Disease Ontology
32 terms(s) returned
| Term Type: | Record: 1 to 32 of 32 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- 3-M syndrome
- 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-phosphoglycerate dehydrogenase deficiency
- 3M syndrome 1
- 3M syndrome 2
- 3M syndrome 3
- 3MC syndrome
- 3MC syndrome 1
- 3MC syndrome 2
- 3MC syndrome 3
- 3p- syndrome
- 3p25.3 microdeletion syndrome
- 3q26 microduplication syndrome
- 3q26q27 microdeletion syndrome
- 3q27.3 microdeletion syndrome
