Nervous System Diseases | Page 2

1250 diseases found in 13 pages

A Diseases

Atelosteogenesis type 3 Atkin syndrome Atypical Rett syndrome Autism with port-wine stain Autosomal dominant centronuclear myopathy Autosomal dominant cerebellar ataxia, deafness, and narcolepsy Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons Autosomal dominant deafness-onychodystrophy syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type A Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Autosomal dominant intermediate Charcot-Marie-Tooth disease type C Autosomal dominant intermediate Charcot-Marie-Tooth disease type D Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Autosomal dominant intermediate Charcot-Marie-Tooth disease type F Autosomal dominant leukodystrophy with autonomic disease Autosomal dominant neuronal ceroid lipofuscinosis 4B Autosomal dominant nocturnal frontal lobe epilepsy Autosomal dominant non-syndromic intellectual disability Autosomal dominant optic atrophy plus syndrome Autosomal dominant partial epilepsy with auditory features Autosomal dominant spinal muscular atrophy, lower extremity-predominant 1 Autosomal recessive axonal neuropathy with neuromyotonia Autosomal recessive centronuclear myopathy Autosomal recessive Charcot-Marie-Tooth disease with hoarseness Autosomal recessive intermediate Charcot-Marie-Tooth disease type A Autosomal recessive intermediate Charcot-Marie-Tooth disease type B Autosomal recessive juvenile Parkinson disease Autosomal recessive neuronal ceroid lipofuscinosis 4A Autosomal recessive primary microcephaly Autosomal recessive spastic ataxia 4 Autosomal recessive spastic paraplegia type 49 Autosomal recessive spinocerebellar ataxia 9

B Diseases

B4GALT1-CDG (CDG-IId) Bannayan-Riley-Ruvalcaba syndrome Barth syndrome Battaglia-Neri syndrome Becker muscular dystrophy Behavioral variant of frontotemporal dementia Behçet disease Bell's palsy Benign essential blepharospasm Benign familial neonatal epilepsy Benign familial neonatal-infantile seizures Benign hereditary chorea Benign rolandic epilepsy (BRE) Beta-Propeller Protein-Associated Neurodegeneration Bethlem myopathy Bilateral frontal polymicrogyria Bilateral frontoparietal polymicrogyria Bilateral generalized polymicrogyria Bilateral parasagittal parieto-occipital polymicrogyria Bilateral perisylvian polymicrogyria Binswanger's disease Biotinidase deficiency Biotin-thiamine-responsive basal ganglia disease Birk-Barel syndrome Bixler Christian Gorlin syndrome Blepharonasofacial malformation syndrome Bobble-head doll syndrome Bohring-Opitz syndrome Borjeson-Forssman-Lehmann syndrome Bowen-Conradi syndrome Brachioskeletogenital syndrome Brachydactyly-mesomelia-intellectual disability-heart defects syndrome Brain dopamine-serotonin vesicular transport disease Brain-lung-thyroid syndrome Branchial arch syndrome X-linked Brody myopathy Brooks Wisniewski Brown syndrome Brown-Sequard syndrome Bullous dystrophy hereditary macular type

C Diseases

Cabezas syndrome CADASIL Camptocormism Camptodactyly arthropathy coxa vara pericarditis syndrome CANOMAD syndrome Cantu syndrome Cap myopathy Cardiofaciocutaneous syndrome Carey-Fineman-Ziter syndrome Carney complex Cataract ataxia deafness Catel Manzke syndrome Caudal appendage deafness Caudal regression sequence Central core disease Central nervous system germinoma Central neurocytoma Central pain syndrome Central pontine myelinolysis Cerebellar ataxia and hypogonadotropic hypogonadism Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Cerebellar degeneration Cerebellar hypoplasia Cerebellar hypoplasia tapetoretinal degeneration Cerebellar hypoplasia with endosteal sclerosis Cerebelloparenchymal disorder 3 Cerebellum agenesis hydrocephaly Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Cerebral cavernous malformation

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

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