| 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.
|
valine metabolism disease
|
37870 |
|
|
Bordetella infectious disease
|
37872 |
|
|
congenital, autosomal dominant nystagmus 2
|
C537854 |
|
|
congenital, autosomal dominant nystagmus 3
|
C537855 |
|
|
congenital, autosomal dominant nystagmus 4
|
C537856 |
|
|
larsen syndrome, dominant type
|
C537873 |
|
|
dental pulp diseases
|
D003788 |
|
|
nonautoimmune, autosomal dominant hyperthyroidism
|
C563786 |
|
|
laron type dwarfism 2
|
C537871 |
|
|
disease or disorder of intervertebral joint
|
37847 |
|
|
coronal dentin dysplasias
|
D003784 |
|
|
dentin anomalous dysplasias
|
D003784 |
|
|
childhood testicular embryonal carcinoma
|
3788 |
|
|
C8orf37 cone-rod dystrophy
|
13786 |
|
|
corneal endothelial dystrophy 1, autosomal dominant
|
7378 |
|
