Gm1 gangliosidosis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
GM1 GANGLIOSIDOSIS
MONDO:0018149
GLB1 Causal — ClinGen, GenCC
GM1 GANGLIOSIDOSIS TYPE 1
79255MONDO:0009260
GLB1 Unknown
24156116
GenCC, Orphanet
GM1 GANGLIOSIDOSIS TYPE 2
79256MONDO:0009261ORPHA79256
GLB1 Causal
24156116
ClinVar, GenCC, Orphanet
GM1 GANGLIOSIDOSIS TYPE 3
79257MONDO:0009262
GLB1 Causal
11511921 7586649 12644936 1928092 1606711 10737981 10841810 8199591 8213816 8198123 1907800 1909089 24156116
ClinVar, Disgenet, Orphanet
GM1-GANGLIOSIDOSIS, TYPE I
230500
GLB1 Unknown — HPO
GM1-GANGLIOSIDOSIS, TYPE II
230600
GLB1 Unknown — HPO
GM1-GANGLIOSIDOSIS, TYPE III
230650
GLB1 Unknown — HPO
JUVENILE GM1 GANGLIOSIDOSIS
C0268272
GLB1 Unknown — Disgenet, ClinGen
TMPPE Unknown — Disgenet —
All2 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Gm1 gangliosidosis.
5 View disease cluster →
mucopolysaccharidosis type 4B 1 shared geneGLB1 Related via 1 shared gene including GLB1. Corneal opacity 1 shared geneGLB1 Related via 1 shared gene including GLB1. Mucopolysaccharidosis 2 shared genesGLB1, TMPPE Related via 2 shared genes including GLB1, TMPPE. Progressive intrahepatic cholestasis 1 shared geneGLB1 Related via 1 shared gene including GLB1. Spondyloepiphyseal dysplasia 1 shared geneGLB1 Related via 1 shared gene including GLB1.