Ataxia, Sensory, 1, Autosomal Dominant (SNAX1)

Alias:
Autosomal Dominant Sensory Ataxia 1
Snax1
Adsa
Ataxia, Sensory, Type 1, Autosomal Dominant
Ataxia, Sensory, Autosomal Dominant
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ataxia, Sensory, 1, Autosomal Dominant, also known as autosomal dominant sensory ataxia 1, is related to attention deficit-hyperactivity disorder and pre-eclampsia, and has symptoms including ataxia An important gene associated with Ataxia, Sensory, 1, Autosomal Dominant is RNF170 (Ring Finger Protein 170), and among its related pathways/superpathways is Class I MHC mediated antigen processing and presentation. The drugs Insulin and Insulin, Globin Zinc have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and brain, and related phenotypes are areflexia and hyporeflexia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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11
55
6

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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