Disease Browser
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Parent Node: Spinocerebellar Ataxias (D020754) |
..Starting node ..Spinocerebellar Ataxia And Plaque-Like Deposits (C566671)
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Child Nodes:
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Sister Nodes: |
..Anemia, sideroblastic spinocerebellar ataxia (C536358)
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..Ataxia Telangiectasia (D001260) 6
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..Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism (C565850)
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..Gemignani syndrome (C537678)
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..Machado-Joseph Disease (D017827) 1
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..MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) (OMIM:271245)
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..Spastic Ataxia (C564815)
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..Spastic ataxia Charlevoix-Saguenay type (C536787)
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..Spinocerebellar Ataxia 10 (C566874)
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..Spinocerebellar Ataxia 11 (C565772)
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..Spinocerebellar Ataxia 12 (C565790)
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..Spinocerebellar Ataxia 15 (C564685)
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..Spinocerebellar Ataxia 17 (C564616)
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..Spinocerebellar ataxia 20 (C537199)
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..Spinocerebellar ataxia 25 (C537202)
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..Spinocerebellar ataxia 26 (C537203)
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..Spinocerebellar ataxia 30 (C575214)
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..Spinocerebellar Ataxia 31 (C566146)
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..Spinocerebellar Ataxia And Plaque-Like Deposits (C566671)
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..Spinocerebellar Ataxia with Dysmorphism (C564802)
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..Spinocerebellar Ataxia with Epilepsy (C564395)
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..Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy (C566669)
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..Spinocerebellar Ataxia, Autosomal Recessive 7 (C563753)
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..Spinocerebellar Ataxia, Autosomal Recessive 8 (C565188)
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..Spinocerebellar Ataxia, Autosomal Recessive 9 (C567436)
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..Spinocerebellar Ataxia, X-Linked 1 (C563134)
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..Spinocerebellar Ataxia, X-Linked 5 (C567478)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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