Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 12 (HMND12)

Alias:

Dhmn Vb

Hmn Vb

Dhmn5b

Dsmavb

Hmn5b

Neuronopathy, Distal Hereditary Motor, Harding Type Vb

Neuropathy, Distal Hereditary Motor, Harding Type Vb

Spinal Muscular Atrophy, Distal, Harding Type Vb

Neuronopathy, Distal Hereditary Motor, Type 5b

Neuropathy, Motor, Distal, Hereditary, Type Vb

Distal Hereditary Motor Neuropathy Type Vb

Neuronopathy, Distal Hereditary Motor, 5b

Spinal Muscular Atrophy Distal Type Vb

Hmnd12

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 12, also known as dhmn vb, is related to distal hereditary motor neuronopathy type 5b and spastic paraplegia 17, autosomal dominant. An important gene associated with Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 12 is REEP1 (Receptor Accessory Protein 1). Affiliated tissues include spinal cord.

Related ID：

MALACARDS：NRN068

OMIM：614751

MESH：D009134