| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-13 15:49:09 UTC |
| updated at |
2021-12-13 16:09:58 UTC |
|
Mondo Disease Ontology (Mondo).
Mondo aims to harmonizes disease definitions across the world. For more details on this ontology see:
Mondo website: https://monarch-initiative.github.io/mondo
OBO Foundry Mondo page: http://obofoundry.org/ontology/mondo.html
|
24,745 entries
|
There is 0 pattern entry.
|
2q31.1 microdeletion syndrome
|
0016652 |
|
|
2q31.1 microduplication syndrome
|
0017412 |
|
|
2q33.1 microdeletion syndrome
|
0016653 |
|
|
2q37 microdeletion syndrome
|
0010886 |
|
|
3-M syndrome
|
0007477 |
|
|
3-hydroxy-3-methylglutaric aciduria
|
0009520 |
|
|
3-hydroxy-3-methylglutaryl-CoA synthase deficiency
|
0011614 |
|
|
3-hydroxyacyl-CoA dehydrogenase deficiency
|
0017715 |
|
|
3-hydroxyisobutyric aciduria
|
0009371 |
|
|
3-hydroxyisobutyryl-CoA hydrolase deficiency
|
0009603 |
|
|
3-methylcrotonyl-CoA carboxylase 1 deficiency
|
0008861 |
|
|
3-methylcrotonyl-CoA carboxylase 2 deficiency
|
0008862 |
|
|
3-methylcrotonyl-CoA carboxylase deficiency
|
0018950 |
|
|
3-methylglutaconic aciduria
|
0017359 |
|
|
3-methylglutaconic aciduria type 1
|
0009610 |
|
