SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that this support group organisation focuses on:
Acquired ataxia Adult-onset autosomal recessive cerebellar ataxia Ataxia with vitamin E deficiency Ataxia-deafness-intellectual disability syndrome Ataxia-hypogonadism-choroidal dystrophy syndrome Ataxia-oculomotor apraxia type 1 Ataxia-tapetoretinal degeneration syndrome Ataxia-telangiectasia Ataxia-telangiectasia-like disorder Autosomal dominant cerebellar ataxia Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type II Autosomal dominant cerebellar ataxia type III Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Autosomal dominant spastic ataxia Autosomal dominant spastic ataxia type 1 Autosomal recessive ataxia due to PEX10 deficiency Autosomal recessive ataxia due to ubiquinone deficiency Autosomal recessive ataxia, Beauce type Autosomal recessive cerebellar ataxia Autosomal recessive cerebellar ataxia due to a DNA repair defect Autosomal recessive cerebellar ataxia with late-onset spasticity Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Autosomal recessive cerebellar ataxia-movement disorder syndrome Autosomal recessive cerebellar ataxia-psychomotor delay syndrome Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Autosomal recessive cerebelloparenchymal disorder type 3 Autosomal recessive congenital cerebellar ataxia Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency Autosomal recessive degenerative and progressive cerebellar ataxia Autosomal recessive metabolic cerebellar ataxia Autosomal recessive spastic ataxia Autosomal recessive spastic ataxia of Charlevoix-Saguenay Autosomal recessive spastic ataxia with leukoencephalopathy Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome Autosomal recessive syndromic cerebellar ataxia CAMOS syndrome Cancer-associated retinopathy Cataract-ataxia-deafness syndrome Cerebellar ataxia, Cayman type Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebellar ataxia-hypogonadism syndrome Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia Childhood-onset spasticity with hyperglycinemia Christianson syndrome Classic paraneoplastic limbic encephalitis Dentatorubral pallidoluysian atrophy Dysequilibrium syndrome EAST syndrome Early-onset cerebellar ataxia with retained tendon reflexes Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome Episodic ataxia type 1 Episodic ataxia type 3 Episodic ataxia type 4 Episodic ataxia type 5 Episodic ataxia type 6 Episodic ataxia type 7 Episodic ataxia with slurred speech Familial paroxysmal ataxia Fragile X-associated tremor/ataxia syndrome Friedreich ataxia Hereditary ataxia Hereditary episodic ataxia Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome Infantile-onset autosomal recessive nonprogressive cerebellar ataxia Infantile-onset spinocerebellar ataxia Joubert syndrome Joubert syndrome and related disorders Joubert syndrome with Jeune asphyxiating thoracic dystrophy Joubert syndrome with hepatic defect Joubert syndrome with ocular defect Joubert syndrome with oculorenal defect Joubert syndrome with renal defect Lambert-Eaton myasthenic syndrome Lethal ataxia with deafness and optic atrophy Limbic encephalitis associated with antibodies to cell membrane antigens Limbic encephalitis with LGI1 antibodies Limbic encephalitis with nCMAgs antibodies Machado-Joseph disease type 1 Machado-Joseph disease type 2 Machado-Joseph disease type 3 Marinesco-Sjögren syndrome Multiple system atrophy, cerebellar type Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome Myoclonus-cerebellar ataxia-deafness syndrome NMDA receptor encephalitis Non-hereditary degenerative ataxia Non-progressive cerebellar ataxia with intellectual disability Opsoclonus-myoclonus syndrome Orofaciodigital syndrome type 6 Paraneoplastic limbic encephalitis Paraneoplastic neurologic syndrome Posterior column ataxia-retinitis pigmentosa syndrome Rare ataxia Recessive mitochondrial ataxia syndrome Richards-Rundle syndrome Spastic ataxia Spastic ataxia with congenital miosis Spastic ataxia-corneal dystrophy syndrome Spectrin-associated autosomal recessive cerebellar ataxia Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 12 Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 15/16 Spinocerebellar ataxia type 17 Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 19/22 Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 20 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 23 Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 26 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 28 Spinocerebellar ataxia type 29 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 32 Spinocerebellar ataxia type 34 Spinocerebellar ataxia type 35 Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 37 Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 7 Spinocerebellar ataxia type 8 Spinocerebellar ataxia with axonal neuropathy type 1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia-dysmorphism syndrome Spinocerebellar degeneration-corneal dystrophy syndrome Sporadic adult-onset ataxia of unknown etiology Steroid-responsive encephalopathy associated with autoimmune thyroiditis Superficial siderosis X-linked cerebellar ataxia X-linked intellectual disability-ataxia-apraxia syndrome X-linked non progressive cerebellar ataxia X-linked progressive cerebellar ataxia X-linked sideroblastic anemia and spinocerebellar ataxia X-linked spinocerebellar ataxia type 3 X-linked spinocerebellar ataxia type 4