ICD·index Chapters ENESDE
8B61.4 category

Localised spinal muscular atrophy

Definition

This category comprises a group of disorders with a varied pattern of weakness and autosomal dominant or X-linked recessive inheritance with specific genetic profiles.

Also indexed as

Autosomal dominant benign distal spinal muscular atrophyAutosomal dominant congenital benign spinal muscular atrophyAutosomal recessive distal spinal muscular atrophy type 4Autosomal recessive lower motor neuron disease with childhood onsetBulbospinal muscular atrophyDHMN1 - [Distal hereditary motor neuropathy type 1]DHMN2 - [Distal hereditary motor neuropathy type 2]DHMN5 - [Distal hereditary motor neuropathy type 5]DHMN7 - [Distal hereditary motor neuropathy type 7]Davidenkow DiseaseDistal HMN - [hereditary motor neuropathy]Distal HMN - [hereditary motor neuropathy] autosomal dominantDistal HMN - [hereditary motor neuropathy] autosomal recessiveDistal HMN, X-linkedDistal form of spinal muscular atrophyDistal hereditary motor neuronopathy type 6Distal hereditary motor neuropathyDistal hereditary motor neuropathy type 1Distal hereditary motor neuropathy type 2Distal hereditary motor neuropathy type 3 and type 4Distal hereditary motor neuropathy type 5Distal hereditary motor neuropathy type 7Distal hereditary motor neuropathy, Jerash typeDistal hereditary motor neuropathy, X-linkedDistal hereditary motor neuropathy, autosomal dominantDistal hereditary motor neuropathy, autosomal recessiveDistal spinal muscular atrophy type 2Distal spinal muscular atrophy, X-linkedDistal spinal muscular atrophy, autosomal dominantDistal spinal muscular atrophy, autosomal recessiveFSHSMA - [Facioscapulohumeral form of spinal muscular atrophy]Facioscapulohumeral form of spinal muscular atrophyFacioscapulohumeral form of spinal muscular atrophy with sensory lossKennedy DiseaseLocalised spinal muscular atrophyOculopharyngeal form of spinal muscular atrophyRyukyu type of spinal muscular atrophySMARD - [Spinal muscular atrophy with respiratory distress]SPSMA - [Scapuloperoneal form of spinal muscular atrophy]Scapulohumeral form of spinal muscular atrophyScapuloperoneal form of spinal muscular atrophySevere infantile axonal neuropathy with respiratory failureSpinal and bulbar muscular atrophySpinal muscular atrophy with respiratory distressdSMA3 and dSMA4 - [Distal hereditary motor neuropathy type 3 and type 4]dSMA4 - [Autosomal recessive distal spinal muscular atrophy type 4]localised SMA - [spinal muscular atrophy]

Nearby in Spinal muscular atrophy