Spastic Paraplegia 57, Autosomal Recessive (SPG57)

Alias:

Hereditary Spastic Paraplegia 57

Spg57

Autosomal Recessive Spastic Paraplegia Type 57

Paraplegia, Spastic, Type 57, Autosomal Recessive

Spastic Paraplegia Due to Partial Tfg Deficiency

Autosomal Recessive Spastic Paraplegia 57

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 57, Autosomal Recessive, also known as hereditary spastic paraplegia 57, is related to spasticity and spastic paraplegia 20, autosomal recessive, and has symptoms including unspecified visual loss An important gene associated with Spastic Paraplegia 57, Autosomal Recessive is TFG (Trafficking From ER To Golgi Regulator). Affiliated tissues include eye, and related phenotypes are abnormality of peripheral nerve conduction and difficulty climbing stairs

Related ID：

MALACARDS：SPS137

OMIM：615658

MESH：D015419