Spastic Paraplegia 4, Autosomal Dominant (SPG4)

Alias:

Spg4

Hereditary Spastic Paraplegia 4

Autosomal Dominant Spastic Paraplegia Type 4

Fsp2

Familial Spastic Paraplegia, Autosomal Dominant, 2

Familial Spastic Paraplegia Autosomal Dominant 2

Paraplegia, Spastic, Autosomal Dominant, Type 4

Autosomal Dominant Spastic Paraplegia 4

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 4, Autosomal Dominant, also known as spg4, is related to paraplegia and spastic paraplegia 3, autosomal dominant, and has symptoms including low back pain, urgency of micturition and agitation. An important gene associated with Spastic Paraplegia 4, Autosomal Dominant is SPAST (Spastin), and among its related pathways/superpathways is Platelet Aggregation Inhibitor Pathway, Pharmacodynamics. Affiliated tissues include brain and spinal cord, and related phenotypes are spasticity and babinski sign

Related ID：

MALACARDS：SPS147

OMIM：182601

MESH：D015419