Argininemia
|
(Orphanet:90)
|
Autosomal recessive limb-girdle muscular dystrophy type 2D
|
(Orphanet:62)
|
Autosomal recessive limb-girdle muscular dystrophy type 2E
|
(Orphanet:119)
|
Autosomal recessive spastic paraplegia type 11
|
(Orphanet:2822)
|
Autosomal recessive spastic paraplegia type 24
|
(Orphanet:101004)
|
Autosomal recessive spastic paraplegia type 45
|
(Orphanet:320396)
|
Hyperornithinemia-hyperammonemia-homocitrullinuria
|
(Orphanet:415)
|
Pachygyria - epilepsy - intellectual deficit - dysmorphism
|
(Orphanet:94084)
|
Spastic paraplegia 64, autosomal recessive
|
(OMIM:615683)
|
X-linked Emery-Dreifuss muscular dystrophy
|
(Orphanet:98863)
|