Frontotemporal dementia with or without amyotrophic lateral sclerosis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS
MONDO:0030923
GRN Unknown
16862115 16862116 16950801 17371905 17436289 17984093 18183624 18184915 23063362 23516300 23596077 29874572 32772750
ClinGen, Disgenet
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2
C4014648
SPG7 Unknown — Disgenet
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3
C4225326
GRN Unknown — Disgenet
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4
C4225325
KIF5A Unknown — Disgenet
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 9
616208OMIM:616208
TUBA4A Unknown — CTD, HPO
All12 Causal8 Unknown4
Related Diseases Diseases that share the most curated genes with Frontotemporal dementia with or without amyotrophic lateral sclerosis.
5 View disease cluster →
Frontotemporal dementia with motor neuron disease 6 shared genesVCP, GRN, SQSTM1, C9orf72, CHCHD10, TBK1 Related via 6 shared genes including VCP, GRN, SQSTM1. Distal myopathy 2 shared genesVCP, SQSTM1 Related via 2 shared genes including VCP, SQSTM1. inclusion body myopathy with Paget disease of bone and frontotemporal dementia 1 shared geneVCP Related via 1 shared gene including VCP. frontotemporal dementia and/or amyotrophic lateral sclerosis 1 shared geneGRN Related via 1 shared gene including GRN. frontotemporal dementia and/or amyotrophic lateral sclerosis 3 1 shared geneSQSTM1 Related via 1 shared gene including SQSTM1.