|
Gamstorp-Wohlfart syndrome
|
7646 |
|
|
miyoshi muscular dystrophy 2
|
C567646 |
|
|
autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
|
7646 |
|
|
myokymia, myotonia and muscle wasting
|
7646 |
|
|
myokymia, myotonia, and muscle wasting
|
7646 |
|
|
autosomal recessive axonal neuropathy with neuromyotonia
|
7646 |
|
|
neuromyotonia and axonal neuropathy, autosomal recessive
|
7646 |
|
|
neuromyotonia and axonal neuropathy, autosomal recessive; NMAN
|
http://purl.obolibrary.org/obo/MONDO_0007646 |
|
|
neurodegenerative disease with chorea
|
17646 |
|
