AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
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(OMIM:608030)
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AMYOTROPHIC LATERAL SCLEROSIS 8
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(OMIM:608627)
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Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
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(Orphanet:313808)
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Alpers syndrome
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(Orphanet:726)
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Behavioral variant of frontotemporal dementia
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(Orphanet:275864)
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Christianson syndrome
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(Orphanet:85278)
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Classical progressive supranuclear palsy
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(Orphanet:240071)
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Congenital neuronal ceroid lipofuscinosis
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(Orphanet:168486)
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ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY
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(OMIM:615924)
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14
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(OMIM:614959)
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Encephalopathy due to prosaposin deficiency
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(Orphanet:139406)
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FRONTOTEMPORAL DEMENTIA
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(OMIM:600274)
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FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1
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(OMIM:105550)
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Familial encephalopathy with neuroserpin inclusion bodies
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(Orphanet:85110)
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Fatal familial insomnia
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(Orphanet:466)
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Fatal infantile cytochrome C oxidase deficiency
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(Orphanet:1561)
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Frontotemporal dementia
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(Orphanet:282)
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Frontotemporal dementia with motor neuron disease
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(Orphanet:275872)
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Huntington disease
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(Orphanet:399)
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Infantile neuroaxonal dystrophy
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(Orphanet:35069)
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Juvenile Huntington disease
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(Orphanet:248111)
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Lissencephaly type 3 - metacarpal bone dysplasia
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(Orphanet:86822)
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McLeod neuroacanthocytosis syndrome
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(Orphanet:59306)
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Multiple congenital anomalies-hypotonia-seizures syndrome type 2
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(Orphanet:300496)
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NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A
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(OMIM:256600)
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NIEMANN-PICK DISEASE, TYPE C1
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(OMIM:257220)
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PARKINSON DISEASE, LATE-ONSET
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(OMIM:168600)
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PEHO syndrome
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(Orphanet:2836)
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PICK DISEASE OF BRAIN
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(OMIM:172700)
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Progressive non-fluent aphasia
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(Orphanet:100070)
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RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL
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(OMIM:614498)
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Recessive mitochondrial ataxia syndrome
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(Orphanet:94125)
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SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL
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(OMIM:602613)
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SUPRANUCLEAR PALSY, PROGRESSIVE, 2
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(OMIM:609454)
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Spinocerebellar ataxia type 17
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(Orphanet:98759)
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Spinocerebellar ataxia type 23
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(Orphanet:101108)
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X-linked spinocerebellar ataxia type 3
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(Orphanet:85297)
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