Spastic Paraplegia 10, Autosomal Dominant (SPG10)

Alias:

Spg10

Hereditary Spastic Paraplegia 10

Autosomal Dominant Spastic Paraplegia Type 10

Spastic Paraplegia 10 with or Without Peripheral Neuropathy

Paraplegia, Spastic, Autosomal Dominant, Type 10

Autosomal Dominant Spastic Paraplegia 10

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 10, Autosomal Dominant, also known as spg10, is related to neuropathy and spasticity, and has symptoms including urgency of micturition An important gene associated with Spastic Paraplegia 10, Autosomal Dominant is KIF5A (Kinesin Family Member 5A), and among its related pathways/superpathways is Insulin processing. Affiliated tissues include brain and spinal cord, and related phenotypes are lower limb spasticity and distal lower limb amyotrophy

Related ID：

MALACARDS：SPS117

OMIM：604187

MESH：D015419