| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
centronuclear myopathy, autosomal, modifier of
|
C4551952 |
|
|
Autosomal dominant centronuclear myopathy
|
C4551952 |
|
|
autosomal dominant centronuclear myopathy
|
C4551952 |
|
|
autosomal dominant centronuclear myopathy caused by mutation in MYF6
|
C4551952 |
|
|
DNM2-related centronuclear myopathy
|
C4551952 |
|
|
myopathy, centronuclear, type 1
|
C4551952 |
|
|
myopathy, centronuclear, type 3
|
C4551952 |
|
