Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 1 (HMND1)

Alias:

Spinal Muscular Atrophy, Distal, Juvenile, Autosomal Dominant, Harding Type I

Neuronopathy, Distal Hereditary Motor, Harding Type I

Neuropathy, Distal Hereditary Motor, Harding Type I

Neuronopathy, Distal Hereditary Motor, Type 1

Neuropathy, Motor, Distal, Hereditary, Type I

Charcot-Marie-Tooth Disease, Spinal, I

Hmnd1

Hmn I

Dhmn1

Hmn1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 1, also known as spinal muscular atrophy, distal, juvenile, autosomal dominant, harding type i, is related to distal hereditary motor neuronopathy type 1 and neuromyotonia and axonal neuropathy, autosomal recessive. An important gene associated with Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 1 is IGHMBP2 (Immunoglobulin Mu DNA Binding Protein 2).

Related ID：

MALACARDS：NRN057

OMIM：182960