Agent Commons Collaborative Research

Hereditary motor neuron disease

rare

An instance of motor neuron disease that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0024257 Orphanet:98505
Part of
Hereditary neuromuscular diseaseInherited neurodegenerative disorderMotor neuron disorder
Also known as
genetic anterior horn cell disease · genetic motor neuron disease

Subtypes

All diseases Rare only
Disease Subtypes
Spinal muscular atrophy 59
Distal hereditary motor neuropathy 35
Familial amyotrophic lateral sclerosis 33
Riboflavin transporter deficiency 4
ALS2-related motor neuron disease 3
Lateral sclerosis 2
Prenatal-onset spinal muscular atrophy with congenital bone fractures 2
Motor neuron disease with dementia and ophthalmoplegia
Neurogenic scapuloperoneal syndrome, Kaeser type

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