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hereditary ataxia

Disease Summary
Associated Targets (214)
Tbio

160

Tchem

30

Tclin

13

Tdark

11


Explore Associated Targets
Mondo Description An instance of an atactic disorder that is caused by an inherited genomic modification in an individual.
Disease Ontology Description A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
Mondo Term and Equivalent IDs
MONDO:0100309:  hereditary ataxia
DOID:0050951: hereditary ataxia
GARD:0006614: 
GARD:0010748: 
ICD10:G11: 
MESH:C531684: 
Orphanet:183518: 
SCTID:763597000: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
genetic nervous system disorder (6096)
Tbio

4331

Tchem

803

Tdark

604

Tclin

358

atactic disorder (216)
Tbio

161

Tchem

30

Tclin

14

Tdark

11

Children
hereditary cerebellar ataxia (196)
Tbio

145

Tchem

28

Tclin

12

Tdark

11

spastic ataxia (9)
Tbio

9

hereditary episodic ataxia (5)
Tchem

3

Tclin

1

Tbio

1

EAST syndrome (2)
Tbio

2

ataxia-hypogonadism-choroidal dystrophy syndrome (1)
Tbio

1

hereditary spastic paraplegia 7 (1)
Tbio

1

autosomal dominant sensory ataxia 1 (1)
Tbio

1

juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome (1)
Tbio

1

mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome (1)
Tbio

1

ataxia with fasciculations (0)
muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome (0)
myoclonus-cerebellar ataxia-deafness syndrome (0)
cataract-ataxia-deafness syndrome (0)
ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome (0)
Richards-Rundle syndrome (0)
spinocerebellar ataxia-dysmorphism syndrome (0)
ataxia-tapetoretinal degeneration syndrome (0)
ataxia-photosensitivity-short stature syndrome (0)
severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome (0)
tremor-ataxia-central hypomyelination syndrome (0)
hypomyelination of early myelinating structures (0)
Target Novelty (Tin-x)