Spastic Paraplegia 72a, Autosomal Dominant (SPG72A)

Alias:

Spastic Paraplegia 72, Autosomal Dominant

Spastic Paraplegia 72, Autosomal Recessive

Paraplegia, Spastic, Type 72, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia 72

Autosomal Dominant Spastic Paraplegia 72

Hereditary Spastic Paraplegia 72

Spastic Paraplegia 72

Spg72a

Spg72

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 72a, Autosomal Dominant, also known as spastic paraplegia 72, autosomal dominant, is related to hereditary spastic paraplegia 72a and amyotrophic lateral sclerosis 1, and has symptoms including muscular stiffness An important gene associated with Spastic Paraplegia 72a, Autosomal Dominant is REEP2 (Receptor Accessory Protein 2). Related phenotypes are urinary bladder sphincter dysfunction and babinski sign

Related ID：

MALACARDS：SPS262

OMIM：615625

MESH：D015419