|
autosomal recessive congenital hypomyelinating neuropathy
|
11527 |
|
|
NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE
|
11527 |
|
|
Charcot Marie Tooth disease type 4E
|
11527 |
|
|
hypomyelination, Severe congenital
|
11527 |
|
|
autosomal recessive congenital hypomyelinating or amyelinating neuropathy
|
11527 |
|
|
neuropathy, congenital hypomyelinating
|
11527 |
|
|
neuropathy, congenital hypomyelinating or AMYELINATING, autosomal recessive
|
11527 |
|
|
neuropathy, congenital hypomyelinating or AMYELINATING, autosomal recessive; CHN
|
http://purl.obolibrary.org/obo/MONDO_0011527 |
|
|
neuropathy, congenital hypomyelinating, 1
|
11527 |
|
|
neuropathy, congenital hypomyelinating, autosomal dominant
|
11527 |
|
