Additional Disease Briefs
Also known as:
HMN8, autosomal dominant benign distal spinal muscular atrophy, autosomal dominant congenital benign spinal muscular atrophy, congenital benign spinal muscular atrophy with contractures, congenital nonprogressive spinal muscular atrophy, neuronopathy, distal hereditary motor, type 8, neuronopathy, distal hereditary motor, type VIII, neuropathy, distal hereditary motor, type 8, spinal muscular atrophy, congenital benign, with contractures, spinal muscular atrophy, distal, congenital nonprogressive
Also known as:
autosomal recessive dHMN, autosomal recessive dSMA, autosomal recessive distal hereditary motor neuropathy, autosomal recessive distal spinal muscular atrophy, distal hereditary motor neuropathy, autosomal recessive
Also known as:
HMN 3, HMN 4, autosomal recessive distal spinal muscular atrophy type 3, dHMN3, dHMN3 and dHMN4, dHMN4, dSMA3, distal hereditary motor neuropathy type 3 and type 4, distal spinal muscular atrophy type 3, neuronopathy, distal hereditary motor, type 3, neuronopathy, distal hereditary motor, type 4, neuropathy, distal hereditary motor, type 4, spinal muscular atrophy, chronic distal, autosomal recessive, spinal muscular atrophy, distal, autosomal recessive, 3
Also known as:
DSMA4, autosomal recessive distal spinal muscular atrophy type 4, autosomal recessive lower motor neuron disease with childhood onset, dSMA4, distal spinal muscular atrophy type 4, neuronopathy, distal hereditary motor, autosomal recessive 4, spinal muscular atrophy, distal, autosomal recessive, 4, spinal muscular atrophy, distal, autosomal recessive, type 4
Also known as:
DSMA5, Young adult-onset dHMN, autosomal recessive distal spinal muscular atrophy type 5, dSMA5, spinal muscular atrophy, distal, autosomal recessive, 5, spinal muscular atrophy, distal, autosomal recessive, type 5, young adult-onset distal hereditary motor neuropathy
Also known as:
Charcot-Marie-Tooth disease, spinal, 2A, HMN 2A, HMN2A, HSPB8 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in HSPB8, neuronopathy, distal hereditary motor, type IIA, neuropathy, distal hereditary motor, type 2A, spinal muscular atrophy, distal, adult, autosomal dominant, 2A
Also known as:
HMN 2B, HMN2B, HSPB1 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in HSPB1, neuronopathy, distal hereditary motor, type IIB, neuropathy, distal hereditary motor, type 2B
Also known as:
HMN 2C, HMN2C, HSPB3 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in HSPB3, neuronopathy, distal hereditary motor, type IIC, neuropathy, distal hereditary motor, type 2C
Also known as:
FBXO38 neuronopathy, distal hereditary motor, HMN 2D, HMN2D, neuronopathy, distal hereditary motor caused by mutation in FBXO38, neuronopathy, distal hereditary motor, type IID, neuropathy, distal hereditary motor, type 2D, spinal muscular atrophy, distal, autosomal dominant, calf-predominant
Also known as:
dHMN5, distal HMN V, distal hereditary motor neuropathy type V, distal spinal muscular atrophy type 5
