Spinocerebellar Ataxia, Autosomal Recessive 7 (SCAR7)

Alias:

Scar7

Autosomal Recessive Spinocerebellar Ataxia 7

Childhood-Onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia

Autosomal Recessive Spinocerebellar Ataxia Type 7

Ataxia, Spinocerebellar, Autosomal Recessive, Type 7

Spinocerebellar Ataxia, Autosomal Recessive, 7

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spinocerebellar Ataxia, Autosomal Recessive 7, also known as scar7, is related to ceroid lipofuscinosis, neuronal, 1 and ceroid lipofuscinosis, neuronal, 6a, and has symptoms including cerebellar ataxia, static tremor and gait ataxia. An important gene associated with Spinocerebellar Ataxia, Autosomal Recessive 7 is TPP1 (Tripeptidyl Peptidase 1). Affiliated tissues include eye and spinal cord, and related phenotypes are progressive cerebellar ataxia and hyperreflexia

Related ID：

MALACARDS：SPN201

OMIM：609270

MESH：D002524