Spastic Paraplegia 11, Autosomal Recessive (SPG11)

Alias:

Spg11

Hereditary Spastic Paraplegia 11

Spastic Paraplegia-Intellectual Disability-Thin Corpus Callosum Syndrome

Autosomal Recessive Spastic Paraplegia Type 11

Nakamura-Osame Syndrome

Hsp-Tcc

Spastic Paraplegia, Autosomal Recessive, with Mental Impairment and Thin Corpus Callosum

Autosomal Recessive Spastic Paraplegia with Mental Impairment and Thin Corpus Callosum

Spastic Paraplegia Autosomal Recessive with Mental Impairment and Thin Corpus Callosum

Spastic Paraplegia, Autosomal Recessive, Complicated, with Thin Corpus Callosum

Autosomal Recessive Spastic Paraplegia Complicated with Thin Corpus Callosum

Spastic Paraplegia Autosomal Recessive Complicated with Thin Corpus Callosum

Autosomal Recessive Spastic Paraplegia with Thinning of Corpus Callosum

Paraplegia, Spastic, Autosomal Recessive, Type 11

Autosomal Recessive Spastic Paraplegia 11

Nakamura Osame Syndrome

Arhsp-Tcc

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 11, Autosomal Recessive, also known as spg11, is related to spastic paraplegia 11 and spastic paraparesis, and has symptoms including ataxia, urgency of micturition and abnormal pyramidal signs. An important gene associated with Spastic Paraplegia 11, Autosomal Recessive is SPG11 (SPG11 Vesicle Trafficking Associated, Spatacsin). Affiliated tissues include brain and spinal cord, and related phenotypes are intellectual disability, mild and specific learning disability

Related ID：

MALACARDS：SPS151

OMIM：604360

MESH：D015419