Agent Commons Collaborative Research

Hereditary ataxia

rare

An instance of an atactic disorder that is caused by an inherited genomic modification in an individual.

Identifiers
MONDO:0100309 Orphanet:183518
Part of
Atactic disorderHereditary neurological disease
Also known as
rare hereditary ataxia · SCA

Subtypes

All diseases Rare only
Disease Subtypes
Hereditary cerebellar ataxia 170
Spastic ataxia 16
Hereditary episodic ataxia 9
EAST syndrome
Richards-Rundle syndrome
Ataxia with fasciculations
Ataxia-hypogonadism-choroidal dystrophy syndrome
Ataxia-tapetoretinal degeneration syndrome
Autosomal dominant sensory ataxia 1
Autosomal recessive ataxia due to PEX16 deficiency
Autosomal recessive ataxia due to PEX2 deficiency
Cataract-ataxia-deafness syndrome
Hereditary spastic paraplegia 7
Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome
Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
Myoclonus-cerebellar ataxia-deafness syndrome
Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome
Spinocerebellar ataxia-dysmorphism syndrome
Tremor-ataxia-central hypomyelination syndrome

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.