Autosomal dominant proximal spinal muscular atrophy

Orpha code: 211037OMIM code:

Definition

A group of rare, genetic, motor neuron disease characterized by childhood or adult onset progressive, predominantly proximal, muscular weakness and wasting. Included diseases are Autosomal dominant adult-onset proximal spinal muscular atrophy, Lower motor neuron syndrome with late-adult onset, and Autosomal dominant childhood-onset proximal spinal muscular atrophy.

Disease data
Classification

Clinical group

ORPHA code
211037
OMIM code
-
ICD10 code
G12.1
ICD11 code
-

No additional description.

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