| 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.
|
centronuclear myopathy 1
|
8048 |
|
|
myopathy, centronuclear, 1
|
8048 |
|
|
trisomy 17p chromosome 17
|
C538048 |
|
|
autosomal dominant centronuclear myopathy
|
8048 |
|
|
centronuclear myopathy, autosomal dominant
|
8048 |
|
|
myopathy, centronuclear, autosomal dominant
|
8048 |
|
|
myotubular myopathy, autosomal dominant
|
8048 |
|
|
cancer of the lip
|
D008048 |
|
|
sudden unexpected death in epilepsy
|
D000080485 |
|
|
DNM2-related centronuclear myopathy
|
8048 |
|
|
myopathy, centronuclear, type 1
|
8048 |
|
|
heparin-induced thrombocytopenia type 2
|
18048 |
|
|
chromosome 17, trisomy 17p
|
C538048 |
|
