ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION
|
(OMIM:270500)
|
Autosomal dominant spastic paraplegia type 10
|
(Orphanet:100991)
|
Autosomal dominant spastic paraplegia type 12
|
(Orphanet:100993)
|
Autosomal dominant spastic paraplegia type 19
|
(Orphanet:100999)
|
Autosomal dominant spastic paraplegia type 31
|
(Orphanet:101011)
|
Autosomal dominant spastic paraplegia type 37
|
(Orphanet:171612)
|
Autosomal dominant spastic paraplegia type 4
|
(Orphanet:100985)
|
Autosomal dominant spastic paraplegia type 6
|
(Orphanet:100988)
|
Autosomal recessive spastic paraplegia type 11
|
(Orphanet:2822)
|
Autosomal recessive spastic paraplegia type 15
|
(Orphanet:100996)
|
Autosomal recessive spastic paraplegia type 20
|
(Orphanet:101000)
|
Autosomal recessive spastic paraplegia type 30
|
(Orphanet:101010)
|
Autosomal recessive spastic paraplegia type 32
|
(Orphanet:171622)
|
Autosomal recessive spastic paraplegia type 35
|
(Orphanet:171629)
|
Autosomal recessive spastic paraplegia type 45
|
(Orphanet:320396)
|
Autosomal recessive spastic paraplegia type 46
|
(Orphanet:320391)
|
BROWN-VIALETTO-VAN LAERE SYNDROME 1
|
(OMIM:211530)
|
Bilateral frontoparietal polymicrogyria
|
(Orphanet:101070)
|
CAMOS syndrome
|
(Orphanet:83472)
|
CHROMOSOME 17p13.1 DELETION SYNDROME
|
(OMIM:613776)
|
Classical phenylketonuria
|
(Orphanet:79254)
|
HYPERREFLEXIA
|
(OMIM:145290)
|
Hyperornithinemia-hyperammonemia-homocitrullinuria
|
(Orphanet:415)
|
Leber plus disease
|
(Orphanet:99718)
|
Pontine tegmental cap dysplasia
|
(Orphanet:269229)
|
Riboflavin transporter deficiency
|
(Orphanet:97229)
|
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION
|
(OMIM:607565)
|
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16
|
(OMIM:615768)
|
Spastic paraplegia 33, autosomal dominant
|
(OMIM:610244)
|
Spondyloepiphyseal dysplasia, Reardon type
|
(Orphanet:163662)
|
WARBURG MICRO SYNDROME 3
|
(OMIM:614222)
|