Distal Hereditary Motor Neuronopathy Type 1 (DHMN1)

Alias:

Autosomal Dominant Distal Juvenile Spinal Muscular Atrophy Type 1

Neuronopathy, Distal Hereditary Motor, Type 1

Neuronopathy, Distal Hereditary Motor, Type I

Dhmn1

Distal Hereditary Motor Neuropathy Type I

Distal Hereditary Motor Neuropathy Type 1

Spinal Charcot-Marie-Tooth Disease 1

Hmn I

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Distal Hereditary Motor Neuronopathy Type 1, also known as autosomal dominant distal juvenile spinal muscular atrophy type 1, is related to neuronopathy, distal hereditary motor, autosomal dominant 1 and charcot-marie-tooth hereditary neuropathy. An important gene associated with Distal Hereditary Motor Neuronopathy Type 1 is IGHMBP2 (Immunoglobulin Mu DNA Binding Protein 2). Related phenotypes are upper limb muscle weakness and hypertonia

Related ID：

MALACARDS：DST141

MESH：C566675