AICARDI-GOUTIERES SYNDROME 2
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(OMIM:610181)
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AMYOTROPHIC DYSTONIC PARAPLEGIA
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(OMIM:105300)
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Allan-Herndon-Dudley syndrome
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(Orphanet:59)
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Argininemia
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(Orphanet:90)
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Autosomal dominant spastic ataxia 1
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(Orphanet:251282)
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Autosomal dominant spastic paraplegia type 10
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(Orphanet:100991)
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Autosomal dominant spastic paraplegia type 12
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(Orphanet:100993)
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Autosomal dominant spastic paraplegia type 13
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(Orphanet:100994)
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Autosomal dominant spastic paraplegia type 17
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(Orphanet:100998)
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Autosomal dominant spastic paraplegia type 19
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(Orphanet:100999)
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Autosomal dominant spastic paraplegia type 29
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(Orphanet:101009)
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Autosomal dominant spastic paraplegia type 3
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(Orphanet:100984)
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Autosomal dominant spastic paraplegia type 31
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(Orphanet:101011)
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Autosomal dominant spastic paraplegia type 36
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(Orphanet:320365)
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Autosomal dominant spastic paraplegia type 37
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(Orphanet:171612)
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Autosomal dominant spastic paraplegia type 38
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(Orphanet:171617)
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Autosomal dominant spastic paraplegia type 4
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(Orphanet:100985)
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Autosomal dominant spastic paraplegia type 41
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(Orphanet:320355)
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Autosomal dominant spastic paraplegia type 42
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(Orphanet:171863)
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Autosomal dominant spastic paraplegia type 6
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(Orphanet:100988)
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Autosomal dominant spastic paraplegia type 8
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(Orphanet:100989)
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Autosomal dominant spastic paraplegia type 9
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(Orphanet:100990)
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Autosomal recessive spastic paraplegia type 11
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(Orphanet:2822)
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Autosomal recessive spastic paraplegia type 14
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(Orphanet:100995)
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Autosomal recessive spastic paraplegia type 15
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(Orphanet:100996)
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Autosomal recessive spastic paraplegia type 18
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(Orphanet:209951)
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Autosomal recessive spastic paraplegia type 20
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(Orphanet:101000)
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Autosomal recessive spastic paraplegia type 21
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(Orphanet:101001)
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Autosomal recessive spastic paraplegia type 23
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(Orphanet:101003)
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Autosomal recessive spastic paraplegia type 24
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(Orphanet:101004)
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Autosomal recessive spastic paraplegia type 26
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(Orphanet:101006)
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Autosomal recessive spastic paraplegia type 27
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(Orphanet:101007)
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Autosomal recessive spastic paraplegia type 28
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(Orphanet:101008)
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Autosomal recessive spastic paraplegia type 30
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(Orphanet:101010)
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Autosomal recessive spastic paraplegia type 32
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(Orphanet:171622)
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Autosomal recessive spastic paraplegia type 35
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(Orphanet:171629)
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Autosomal recessive spastic paraplegia type 43
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(Orphanet:320370)
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Autosomal recessive spastic paraplegia type 44
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(Orphanet:320401)
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Autosomal recessive spastic paraplegia type 45
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(Orphanet:320396)
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Autosomal recessive spastic paraplegia type 46
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(Orphanet:320391)
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Autosomal recessive spastic paraplegia type 48
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(Orphanet:306511)
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Autosomal recessive spastic paraplegia type 49
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(Orphanet:320385)
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Autosomal recessive spastic paraplegia type 53
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(Orphanet:319199)
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Autosomal recessive spastic paraplegia type 54
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(Orphanet:320380)
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Autosomal recessive spastic paraplegia type 55
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(Orphanet:320375)
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Autosomal recessive spastic paraplegia type 56
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(Orphanet:320411)
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Autosomal recessive spastic paraplegia type 5A
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(Orphanet:100986)
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Autosomal recessive spastic paraplegia type 7
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(Orphanet:99013)
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Behr syndrome
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(Orphanet:1239)
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CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE
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(OMIM:302700)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4
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(OMIM:612164)
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Generalized congenital lipodystrophy with myopathy
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(Orphanet:228429)
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Giant axonal neuropathy
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(Orphanet:643)
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Hereditary sensory and autonomic neuropathy with spastic paraplegia
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(Orphanet:139578)
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Homocarnosinosis
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(Orphanet:2168)
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Hydrocephalus with stenosis of aqueduct of Sylvius
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(Orphanet:2182)
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Infantile-onset ascending hereditary spastic paralysis
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(Orphanet:293168)
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Intellectual deficit - spasticity - ectrodactyly
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(Orphanet:1891)
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KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA
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(OMIM:308750)
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Laurence-Moon syndrome
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(Orphanet:2377)
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Leukoencephalopathy - metaphyseal chondrodysplasia
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(Orphanet:83629)
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MASA syndrome
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(Orphanet:2466)
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METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA
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(OMIM:250500)
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Macrocephaly - spastic paraplegia - dysmorphism
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(Orphanet:2429)
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OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME
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(OMIM:311100)
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Paraplegia - intellectual deficit - hyperkeratosis
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(Orphanet:2824)
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Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
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(Orphanet:53583)
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Pontocerebellar hypoplasia type 7
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(Orphanet:284339)
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Pyruvate dehydrogenase E3-binding protein deficiency
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(Orphanet:255182)
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SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE
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(OMIM:614066)
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SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
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(OMIM:613744)
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SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
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(OMIM:614067)
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SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE
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(OMIM:615658)
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SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE
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(OMIM:615685)
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SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE
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(OMIM:615625)
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SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT
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(OMIM:616282)
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SPASTIC PARAPLEGIA AND EVANS SYNDROME
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(OMIM:601608)
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SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS
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(OMIM:182800)
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SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION
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(OMIM:607565)
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SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA
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(OMIM:182830)
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Severe intellectual deficit and progressive spastic paraplegia
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(Orphanet:280763)
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Spastic paraplegia - epilepsy - intellectual deficit
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(Orphanet:2816)
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Spastic paraplegia - glaucoma - intellectual deficit
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(Orphanet:2818)
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Spastic paraplegia - nephritis - deafness
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(Orphanet:2820)
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Spastic paraplegia - neuropathy - poikiloderma
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(Orphanet:2821)
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Spastic paraplegia - precocious puberty
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(Orphanet:2826)
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Spastic paraplegia 33, autosomal dominant
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(OMIM:610244)
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Spastic paraplegia 63, autosomal recessive
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(OMIM:615686)
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Spastic paraplegia 64, autosomal recessive
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(OMIM:615683)
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Spastic paraplegia type 2
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(Orphanet:99015)
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Spastic paraplegia-optic atrophy-neuropathy syndrome
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(Orphanet:320406)
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Waardenburg syndrome
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(Orphanet:3440)
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X-linked cerebral adrenoleukodystrophy
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(Orphanet:139396)
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X-linked immunoneurologic disorder
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(Orphanet:2571)
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X-linked spastic paraplegia type 16
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(Orphanet:100997)
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X-linked spastic paraplegia type 34
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(Orphanet:171607)
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[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
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(OMIM:607259)
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