Hereditary Spastic Paraplegia 72a (SPG72)

Alias:

Autosomal Spastic Paraplegia Type 72

Spg72

Hereditary Spastic Paraplegia 72

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hereditary Spastic Paraplegia 72a, also known as autosomal spastic paraplegia type 72, is related to spastic paraplegia 72a, autosomal dominant and amyotrophic lateral sclerosis 1. An important gene associated with Hereditary Spastic Paraplegia 72a is REEP2 (Receptor Accessory Protein 2). Related phenotypes are spastic gait and rigidity

Related ID：

MALACARDS：HRD241