Hereditary Sensory and Autonomic Neuropathy Due to Tecpr2 Mutation (SPG49)

Alias:

Autosomal Recessive Spastic Paraplegia Type 49

Hsan Due to Tecpr2 Mutation

Spg49

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hereditary Sensory and Autonomic Neuropathy Due to Tecpr2 Mutation, also known as autosomal recessive spastic paraplegia type 49, is related to hereditary spastic paraplegia 49 and spastic paraplegia type 49. An important gene associated with Hereditary Sensory and Autonomic Neuropathy Due to Tecpr2 Mutation is TECPR2 (Tectonin Beta-Propeller Repeat Containing 2). Related phenotypes are recurrent respiratory infections and intellectual disability

Related ID：

MALACARDS：HRD238