Spastic Paraplegia 36, Autosomal Dominant (SPG36)

Alias:

Spg36

Autosomal Dominant Spastic Paraplegia Type 36

Hereditary Spastic Paraplegia 36

Autosomal Dominant Spastic Paraplegia 36

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 36, Autosomal Dominant, also known as spg36, is related to hereditary spastic paraplegia 23 and spastic paraplegia 27, autosomal recessive, and has symptoms including urgency of micturition An important gene associated with Spastic Paraplegia 36, Autosomal Dominant is SPG36 (Spastic Paraplegia 36 (Autosomal Dominant)). Related phenotypes are hyperreflexia and babinski sign

Related ID：

MALACARDS：SPS118

OMIM：613096