Spastic Paraplegia 15 (SPG15)

Alias:

Spg15

Zfyve26-Related Hereditary Spastic Paraplegia

Spastic Paraplegia and Retinal Degeneration

Spastic Paraplegia 15, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia 15

Hereditary Spastic Paraplegia Type 15

Spastic Paraplegia Type 15

Kjellin Syndrome

Hsp-Zfyve26

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 15, also known as spg15, is related to spastic paraplegia 15, autosomal recessive and complex hereditary spastic paraplegia, and has symptoms including ataxia, clonus and urgency of micturition. An important gene associated with Spastic Paraplegia 15 is ZFYVE26 (Zinc Finger FYVE-Type Containing 26). Affiliated tissues include spinal cord and brain.

Related ID：

MALACARDS：SPS025