Deutsche Heredo-Ataxie Gesellschaft e.V. (DHAG) Assigned 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