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Severe neonatal myoclonus
Severe neonatal myoclonus
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
KIF5A-associated severe neonatal myoclonus
MONDO_0014979
KIF5A
Unknown
27463701
27414745
Open Targets
Endocytosis
Dopaminergic synapse
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
Non-small cell lung cancer
MHC class II antigen presentation
RHO GTPases activate KTN1
COPI-dependent Golgi-to-ER retrograde traffic
Kinesins
+12 more
severe neonatal myoclonus
MONDO_0014979
KIF5A
Unknown
22258533
24215330
27414745
27463701
Open Targets
Endocytosis
Dopaminergic synapse
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
Non-small cell lung cancer
MHC class II antigen presentation
RHO GTPases activate KTN1
COPI-dependent Golgi-to-ER retrograde traffic
Kinesins
+12 more
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
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Diseases that share the most curated genes with Severe neonatal myoclonus.
5
View disease cluster →
Amyotrophic lateral sclerosis, susceptibility to, 25
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Inherited neurodegenerative disorder
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Spastic paraplegia 10, autosomal dominant
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Genetic neurodegenerative disease
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Frontotemporal dementia with or without amyotrophic lateral sclerosis
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
1
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