Spastic Paraplegia 43, Autosomal Recessive (SPG43)

Alias:

Hereditary Spastic Paraplegia 43

Spg43

Autosomal Recessive Spastic Paraplegia Type 43

Paraplegia, Spastic, Type 43, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia 43

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 43, Autosomal Recessive, also known as hereditary spastic paraplegia 43, is related to neurodegeneration with brain iron accumulation 4 and neurodegeneration with brain iron accumulation, and has symptoms including muscle spasticity An important gene associated with Spastic Paraplegia 43, Autosomal Recessive is C19orf12 (Chromosome 19 Open Reading Frame 12). Affiliated tissues include brain, and related phenotypes are babinski sign and difficulty walking

Related ID：

MALACARDS：SPS130

OMIM：615043

MESH：D015419