| Disease Browser
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Parent Node:
 Ataxia (D001259) |
..Starting node
.. Myokymia 1 (C567174)
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Child Nodes:
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Sister Nodes: |
..Abetalipoproteinemia neuropathy (C540309)
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..Arts syndrome (C535388)
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..Ataxia and Polyneuropathy, Adult-Onset (C564020)
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..Ataxia with Fasciculations (C566246)
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..Ataxia with Myoclonic Epilepsy and Presenile Dementia (C565933)
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..Ataxia with vitamin E deficiency (C535393)
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..Ataxia, Deafness, and Cardiomyopathy (C565932)
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..ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT (OMIM:608984)
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..Ataxia, Sensory, Autosomal Dominant (C563818)
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..Ataxia, Spastic, with Congenital Miosis (C566247)
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..Ataxia-Microcephaly-Cataract Syndrome (C563086)
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..Atonic-Astatic Syndrome of Foerster (C565926)
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..Bangstad syndrome (C537902)
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..Behr syndrome (C537669)
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..Bhaskar Jagannathan syndrome (C535437)
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..CANOMAD syndrome (C537980)
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..Carnitine Acetyltransferase Deficiency (C563249)
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..Cataract ataxia deafness (C538283)
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..Cataracts, ataxia, short stature, and mental retardation (C535345)
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..Cerebellar Ataxia (D002524)  70
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..Cerebral Palsy, Ataxic, Autosomal Recessive (C562856)
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..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
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..COACH syndrome (C536430)
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..Coenzyme Q10 Deficiency (C564403)
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..COENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
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..Deafness hyperuricemia neurologic ataxia (C535995)
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..Diaminopentanuria (C565630)
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..Episodic Ataxia (C580065)
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..Episodic ataxia with nystagmus (C535506)
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..Episodic Ataxia, Type 1 (C563278)
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..Episodic Ataxia, Type 3 (C564697)
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..Episodic Ataxia, Type 4 (C564698)
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..Episodic Ataxia, Type 7 (C567459)
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..Erythrokeratodermia with ataxia (C535738)
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..Fragile X Tremor Ataxia Syndrome (C564105)
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..Gait Ataxia (D020234)
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..Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response (C537159)
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..Joubert Syndrome 7 (C566916)
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..Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
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..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
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..Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus (C562774)
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..Myokymia 1 (C567174)
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..Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia (C566817)
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..Partington X-linked mental retardation syndrome (C536300)
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..Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (C564894)
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..Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
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..Posterior column ataxia with retinitis pigmentosa (C536343)
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..Reardon Wilson Cavanagh syndrome (C535295)
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..Richards-Rundle syndrome (C535674)
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..SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE (OMIM:613672)
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..Spastic Paraplegia, Ataxia, And Mental Retardation (C564378)
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..Spondyloepimetaphyseal dysplasia, Genevieve type (C535785)
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..Tapetoretinal Degeneration with Ataxia (C564788)
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..Treft Sanborn Carey syndrome (C536544)
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..Tremor of Intention, Ataxia, and Lipofuscinosis (C566038)
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..Tryptophanuria With Dwarfism (C562658)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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