Spastic Paraplegia 31, Autosomal Dominant (SPG31)

Alias:

Spg31

Hereditary Spastic Paraplegia 31

Autosomal Dominant Spastic Paraplegia Type 31

Paraplegia, Spastic, Autosomal Dominant, Type 31

Autosomal Dominant Spastic Paraplegia 31

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 31, Autosomal Dominant, also known as spg31, is related to spastic paraplegia 3a and spastic paraplegia 3, autosomal dominant. An important gene associated with Spastic Paraplegia 31, Autosomal Dominant is REEP1 (Receptor Accessory Protein 1). Affiliated tissues include skeletal muscle and brain, and related phenotypes are proximal muscle weakness in lower limbs and spastic gait

Related ID：

MALACARDS：SPS148

OMIM：610250

MESH：D015419