Spastic Paraplegia 8, Autosomal Dominant (SPG8)

Alias:

Spg8

Hereditary Spastic Paraplegia 8

Autosomal Dominant Spastic Paraplegia Type 8

Paraplegia, Spastic, Autosomal Dominant, Type 8

Autosomal Dominant Spastic Paraplegia 8

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 8, Autosomal Dominant, also known as spg8, is related to spastic paraplegia 8 and spasticity, and has symptoms including urgency of micturition An important gene associated with Spastic Paraplegia 8, Autosomal Dominant is WASHC5 (WASH Complex Subunit 5). Affiliated tissues include eye and spinal cord, and related phenotypes are hyperreflexia and babinski sign

Related ID：

MALACARDS：SPS149

OMIM：603563

MESH：D015419