Tay-sachs disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
TAY-SACHS DISEASE
C0039373272800MESH:D013661MONDO:0010100
GM2A Causal — Disgenet
HEXA Causal
11392526
CTD, ClinGen, ClinVar, Disgenet, GenCC, HPO
TAY-SACHS DISEASE, JUVENILE
C1848913
HEXA Causal — Disgenet
TAY-SACHS DISEASE, VARIANT AB
GM2A Causal
8900233 10364519 26203402
ClinVar
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Tay-sachs disease.
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Gm2 gangliosidosis 2 shared genesHEXA, GM2A Related via 2 shared genes including HEXA, GM2A. Beta-hexosaminidase a deficiency 1 shared geneHEXA Related via 1 shared gene including HEXA. Ataxia with oculomotor apraxia 1 shared geneSETX Related via 1 shared gene including SETX. Proximal spinal muscular atrophy 1 shared geneSETX Related via 1 shared gene including SETX. Leukodystrophy 1 shared geneHEXA Related via 1 shared gene including HEXA.