| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
EBVaGC
|
17784 |
|
|
PRTH
|
7784 |
|
|
gelsolin-related amyloidosis
|
C000657784 |
|
|
kymenlaakso syndrome
|
C000657784 |
|
|
3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency
|
C567784 |
|
|
HMGCS2 deficiency
|
C567784 |
|
|
aortic aneurysm-aortic dissection and patent ductus arteriosus
|
C537784 |
|
|
lattice type II corneal dystrophy
|
C000657784 |
|
|
familial thoracic 4 aortic aneurysm
|
C537784 |
|
|
EBV-associated gastric carcinoma
|
17784 |
|
|
familial amyloidosis, finnish type
|
C000657784 |
|
|
hyperthyroidism, familial, due to inappropriate thyrotropin secretion
|
7784 |
|
|
lattice corneal dystrophy type ii
|
C000657784 |
|
|
lattice corneal dystrophy, gelsolin type
|
C000657784 |
|
|
lattice corneal dystrophy, type II
|
C000657784 |
|
