Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandDyskinesias (D020820)
..Starting node
..expandAtaxia (D001259)

       Child Nodes:
........expandAbetalipoproteinemia neuropathy (C540309)
........expandArts syndrome (C535388)
........expandAtaxia and Polyneuropathy, Adult-Onset (C564020)
........expandAtaxia with Fasciculations (C566246)
........expandAtaxia with Myoclonic Epilepsy and Presenile Dementia (C565933)
........expandAtaxia with vitamin E deficiency (C535393)
........expandAtaxia, Deafness, and Cardiomyopathy (C565932)
........expandATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT (OMIM:608984)
........expandAtaxia, Sensory, Autosomal Dominant (C563818)
........expandAtaxia, Spastic, with Congenital Miosis (C566247)
........expandAtaxia-Microcephaly-Cataract Syndrome (C563086)
........expandAtonic-Astatic Syndrome of Foerster (C565926)
........expandBangstad syndrome (C537902)
........expandBehr syndrome (C537669)
........expandBhaskar Jagannathan syndrome (C535437)
........expandCANOMAD syndrome (C537980)
........expandCarnitine Acetyltransferase Deficiency (C563249)
........expandCataract ataxia deafness (C538283)
........expandCataracts, ataxia, short stature, and mental retardation (C535345)
........expandCerebellar Ataxia (D002524) Child70
........expandCerebral Palsy, Ataxic, Autosomal Recessive (C562856)
........expandCerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
........expandCOACH syndrome (C536430)
........expandCoenzyme Q10 Deficiency (C564403)
........expandCOENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
........expandDeafness hyperuricemia neurologic ataxia (C535995)
........expandDiaminopentanuria (C565630)
........expandEpisodic Ataxia (C580065)
........expandEpisodic ataxia with nystagmus (C535506)
........expandEpisodic Ataxia, Type 1 (C563278)
........expandEpisodic Ataxia, Type 3 (C564697)
........expandEpisodic Ataxia, Type 4 (C564698)
........expandEpisodic Ataxia, Type 7 (C567459)
........expandErythrokeratodermia with ataxia (C535738)
........expandFragile X Tremor Ataxia Syndrome (C564105)
........expandGait Ataxia (D020234)
........expandHypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response (C537159)
........expandJoubert Syndrome 7 (C566916)
........expandLeukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
........expandMental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
........expandMuscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus (C562774)
........expandMyokymia 1 (C567174)
........expandParoxysmal Tonic Upgaze, Benign Childhood, With Ataxia (C566817)
........expandPartington X-linked mental retardation syndrome (C536300)
........expandPeripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (C564894)
........expandPolyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
........expandPosterior column ataxia with retinitis pigmentosa (C536343)
........expandReardon Wilson Cavanagh syndrome (C535295)
........expandRichards-Rundle syndrome (C535674)
........expandSPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE (OMIM:613672)
........expandSpastic Paraplegia, Ataxia, And Mental Retardation (C564378)
........expandSpondyloepimetaphyseal dysplasia, Genevieve type (C535785)
........expandTapetoretinal Degeneration with Ataxia (C564788)
........expandTreft Sanborn Carey syndrome (C536544)
........expandTremor of Intention, Ataxia, and Lipofuscinosis (C566038)
........expandTryptophanuria With Dwarfism (C562658)



 Sister Nodes: 
..expandAtaxia (D001259) Child126
..expandAthetosis (D001264) Child3
..expandBobble-head doll syndrome (C536241)
..expandCatalepsy (D002375)
..expandChorea (D002819) Child17
..expandChoreoathetosis/Spasticity, Episodic (C563401)
..expandDyskinesia, Drug-Induced (D004409)
..expandDyskinesia, Familial, with Facial Myokymia (C564676)
..expandDystonia (D004421) Child18
..expandEpisodic Kinesigenic Dyskinesia 2 (C567026)
..expandHyperkinesis (D006948)
..expandHypokinesia (D018476) Child1
..expandInfantile convulsions and paroxysmal choreoathetosis, familial (C535522)
..expandMental Retardation, X-Linked, Syndromic 10 (C564560)
..expandMicrocephaly pontocerebellar hypoplasia dyskinesia (C537543)
..expandMIRROR MOVEMENTS 1 (OMIM:157600)
..expandMyoclonus (D009207) Child10
..expandParoxysmal Exertion-Induced Dyskinesia And Hemolytic Anemia (C567412)
..expandPsychomotor Agitation (D011595) Child1
..expandSynkinesis (D046608) Child2
..expandTics (D020323)
..expandTremor (D014202) Child6
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:977
Name:Ataxia
Definition:Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.
Alternative IDs:
ParentIDs:MESH:D020820
TreeNumbers:C10.597.350.090 |C23.888.592.350.090
Synonyms:Appendicular Ataxia |Appendicular Ataxias |Ataxia, Appendicular |Ataxia, Limb |Ataxia, Motor |Ataxias |Ataxias, Appendicular |Ataxia, Sensory |Ataxias, Limb |Ataxias, Motor |Ataxias, Sensory |Ataxias, Truncal |Ataxia, Truncal |Ataxy |Coordination Impairment |Coordinati
Slim Mappings:Nervous system disease|Signs and symptoms
Reference: MedGen: D001259
MeSH: D001259
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants