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Disease association ontology term - MONDO:0020128 - motor neuron disorder

Term summary

ID
MONDO:0020128
Name
motor neuron disorder
Ontology or CV name
Disease association
Definition
Neurological disease involving the motor neuron.

Parents

Annotation

Disease association

MONDO:0020128 - motor neuron disorder

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MONDO:0008453 - adult-onset proximal spinal muscular atrophy, autosomal dominant

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MONDO:0004976 - amyotrophic lateral sclerosis

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MONDO:0859529 - amyotrophic lateral sclerosis 27, juvenile

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MONDO:0007103 - amyotrophic lateral sclerosis type 1

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MONDO:0012945 - amyotrophic lateral sclerosis type 11

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MONDO:0010459 - amyotrophic lateral sclerosis type 15

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MONDO:0013715 - amyotrophic lateral sclerosis type 16

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MONDO:0014531 - amyotrophic lateral sclerosis type 22

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MONDO:0011223 - amyotrophic lateral sclerosis type 4

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MONDO:0012077 - amyotrophic lateral sclerosis type 8

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MONDO:0008026 - autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

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MONDO:0011436 - autosomal recessive distal spinal muscular atrophy 1

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MONDO:0011585 - autosomal recessive distal spinal muscular atrophy 2

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MONDO:0014395 - frontotemporal dementia and/or amyotrophic lateral sclerosis 2

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MONDO:0013501 - frontotemporal dementia and/or amyotrophic lateral sclerosis 6

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MONDO:0010936 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7

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MONDO:0010043 - hereditary spastic paraplegia 17

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MONDO:0010532 - infantile-onset X-linked spinal muscular atrophy

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MONDO:0014025 - lower motor neuron syndrome with late-adult onset

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MONDO:0976133 - myopathy, myofibrillar, 13, with rimmed vacuoles

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MONDO:0971150 - neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity

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MONDO:0030055 - neuronopathy, distal hereditary motor, autosomal recessive 8

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MONDO:0957874 - neuronopathy, distal hereditary motor, autosomal recessive 9

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MONDO:0008025 - neuronopathy, distal hereditary motor, type 2A

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MONDO:0012080 - neuronopathy, distal hereditary motor, type 2B

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MONDO:0013243 - neuronopathy, distal hereditary motor, type 2C

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MONDO:0015353 - neuronopathy, distal hereditary motor, type 5A

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MONDO:0013884 - neuronopathy, distal hereditary motor, type 5B

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MONDO:0030860 - neuronopathy, distal hereditary motor, type 5C

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MONDO:0011879 - neuronopathy, distal hereditary motor, type 7B

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MONDO:0060585 - neuronopathy, distal hereditary motor, type 9

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MONDO:0016396 - pontocerebellar hypoplasia type 1

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MONDO:0013853 - pontocerebellar hypoplasia type 1B

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MONDO:0010190 - pontocerebellar hypoplasia type 2A

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MONDO:0012890 - pontocerebellar hypoplasia type 2B

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MONDO:0012891 - pontocerebellar hypoplasia type 2C

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MONDO:0014485 - pontocerebellar hypoplasia, type 1C

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MONDO:0014874 - pontocerebellar hypoplasia, type 2F

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MONDO:0014806 - spinal muscular atrophy with congenital bone fractures 1

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MONDO:0014807 - spinal muscular atrophy with congenital bone fractures 2

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MONDO:0859279 - spinal muscular atrophy, distal, autosomal recessive, 6

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MONDO:0009669 - spinal muscular atrophy, type 1

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MONDO:0009673 - spinal muscular atrophy, type II

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MONDO:0009672 - spinal muscular atrophy, type III

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MONDO:0010056 - spinal muscular atrophy, type IV

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MONDO:0008458 - spinocerebellar ataxia type 2

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MONDO:0010338 - X-linked distal spinal muscular atrophy type 3

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