Human Disease Ontology
22 terms(s) returned
| Term Type: | Record: 1 to 22 of 22 Records | Page: 1 of 1, First Previous Next Last | Show Records Per Page |
- 3-M syndrome
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
- 3-hydroxyisobutryl-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 7a
- 3-methylglutaconic aciduria type 7b
- 3-methylglutaconic aciduria type 8
- 3-methylglutaconic aciduria type 9
- 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- 3MC syndrome
- 3MC syndrome 1
- 3MC syndrome 2
- 3MC syndrome 3
- 3p deletion syndrome
