Nervous System Diseases | Page 9

1250 diseases found in 13 pages

M Diseases

Myotonic dystrophy type 2

N Diseases

Nance-Horan syndrome Narcolepsy NBIA/DYT/PARK-PLA2G6 Necrotizing autoimmune myopathy Neonatal adrenoleukodystrophy Neonatal meningitis Neonatal progeroid syndrome Neu Laxova syndrome Neuroblastoma Neurocutaneous melanosis Neurofaciodigitorenal syndrome Neuroferritinopathy Neurofibromatosis type 1 Neurofibromatosis type 2 Neuroleptic malignant syndrome Neuromyelitis optica Neuromyelitis optica spectrum disorder Neuronal ceroid lipofuscinosis Neuronal ceroid lipofuscinosis 10 Neuronal ceroid lipofuscinosis 2 Neuronal ceroid lipofuscinosis 3 Neuronal ceroid lipofuscinosis 5 Neuronal ceroid lipofuscinosis 6 Neuronal ceroid lipofuscinosis 7 Neuronal ceroid lipofuscinosis 9 Neuronal intranuclear inclusion disease Neuropathy ataxia retinitis pigmentosa syndrome Neuropathy, distal hereditary motor, Jerash type Neuropathy, hereditary motor and sensory, Okinawa type Neuropathy, hereditary motor and sensory, Russe type Neutral lipid storage disease with myopathy Nevoid basal cell carcinoma syndrome New-onset refractory status epilepticus Nicolaides-Baraitser syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Non 24 hour sleep wake disorder Nondystrophic myotonia Noonan syndrome Norrie disease Northern epilepsy N syndrome

O Diseases

Oculocerebrocutaneous syndrome Oculofaciocardiodental syndrome Oculopharyngeal muscular dystrophy Oculopharyngodistal myopathy Okamoto syndrome Olfactory neuroblastoma Oligoastrocytoma Oligodendroglioma Oliver syndrome Olivopontocerebellar atrophy Omphalocele cleft palate syndrome lethal OPHN1 syndrome Opsoclonus-myoclonus syndrome Optic atrophy 2 Optic pathway glioma Ornithine transcarbamylase deficiency Orofaciodigital syndrome 1 Orofaciodigital syndrome 10 Orofaciodigital syndrome 2 Orofaciodigital syndrome 3 Orofaciodigital syndrome 4 Orofaciodigital syndrome 5 Orofaciodigital syndrome 6 Orthostatic intolerance due to NET deficiency Osteopenia and sparse hair Osteoporosis-pseudoglioma syndrome Oto-palato-digital syndrome type 1 Oto-palato-digital syndrome type 2 Ouvrier Billson syndrome

P Diseases

Pachygyria-intellectual disability-epilepsy syndrome PACS1-related syndrome Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Pallidopyramidal syndrome Pallister-Killian mosaic syndrome Pallister W syndrome Pantothenate kinase-associated neurodegeneration Paralysis agitans, juvenile, of Hunt Paramyotonia congenita Parkinson disease type 3 Parkinson disease type 9 Paroxysmal exertion-induced dyskinesia Paroxysmal extreme pain disorder Paroxysmal hemicrania Paroxysmal kinesigenic choreoathetosis Paroxysomal nonkinesigenic dyskinesia Parsonage Turner syndrome Partington syndrome PCDH19-related female-limited epilepsy Pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections PEHO syndrome Pelizaeus-Merzbacher disease Periventricular heterotopia Periventricular leukomalacia Perry syndrome Peters plus syndrome

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

People Using the App

Join the RareGuru Community

To connect, share, empower and heal today.

People Using the App