Spastic Paraplegia 61, Autosomal Recessive (SPG61)

Alias:

Hereditary Spastic Paraplegia 61

Spg61

Autosomal Recessive Spastic Paraplegia Type 61

Paraplegia, Spastic, Type 61, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia 61

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 61, Autosomal Recessive, also known as hereditary spastic paraplegia 61, is related to paraplegia and spastic paraplegia 20, autosomal recessive, and has symptoms including muscle spasticity An important gene associated with Spastic Paraplegia 61, Autosomal Recessive is ARL6IP1 (ADP Ribosylation Factor Like GTPase 6 Interacting Protein 1). Affiliated tissues include liver, and related phenotypes are spasticity and difficulty walking

Related ID：

MALACARDS：SPS141

OMIM：615685

MESH：D015419