Spastic Paraplegia Type 49 (SPG49)

Alias:

Spastic Paraplegia 49, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia Type 49

Spg49

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia Type 49, also known as spastic paraplegia 49, autosomal recessive, is related to hereditary sensory and autonomic neuropathy due to tecpr2 mutation and hereditary spastic paraplegia 49, and has symptoms including gait ataxia An important gene associated with Spastic Paraplegia Type 49 is TECPR2 (Tectonin Beta-Propeller Repeat Containing 2). Affiliated tissues include lung and heart.

Related ID：

MALACARDS：SPS230