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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3076 - 3100 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0110825
  • hereditary spastic paraplegia 9B
  • Aliases:
    • SPG9B
    • autosomal recessive complex spastic paraplegia type 9B
    • autosomal recessive spastic paraplegia 9B
Homo sapiens (human)
DOID:0110795
  • hereditary spastic paraplegia 43
  • Aliases:
    • SPG43
    • autosomal recessive spastic paraplegia 43
    • autosomal recessive spastic paraplegia type 43
Homo sapiens (human)
DOID:0110813
  • hereditary spastic paraplegia 62
  • Aliases:
    • SPG62
    • autosomal recessive spastic paraplegia 62
    • autosomal recessive spastic paraplegia type 62
Homo sapiens (human)
DOID:0110817
  • hereditary spastic paraplegia 72A
  • Aliases:
    • SPG72
    • autosomal spastic paraplegia type 72
Homo sapiens (human)
DOID:0110787
  • hereditary spastic paraplegia 36
  • Aliases:
    • SPG36
    • autosomal dominant spastic paraplegia 36
    • autosomal dominant spastic paraplegia type 36
Homo sapiens (human)
DOID:0110823
  • hereditary spastic paraplegia 8
  • Aliases:
    • SPG8
    • autosomal dominant spastic paraplegia 8
    • autosomal dominant spastic paraplegia type 8
Homo sapiens (human)
DOID:0110792
  • hereditary spastic paraplegia 4
  • Aliases:
    • SPG4
    • autosomal dominant spastic paraplegia 4
    • autosomal dominant spastic paraplegia type 4
Homo sapiens (human)
DOID:0110822
  • hereditary spastic paraplegia 77
  • Aliases:
    • SPG77
    • autosomal recessive spastic paraplegia 77
Homo sapiens (human)
DOID:0110808
  • hereditary spastic paraplegia 56
  • Aliases:
    • SPG56
    • autosomal recessive spastic paraplegia 56
    • autosomal recessive spastic paraplegia type 56
Homo sapiens (human)
DOID:0110767
  • hereditary spastic paraplegia 14
  • Aliases:
    • SPG14
    • autosomal recessive spastic paraplegia 14
    • autosomal recessive spastic paraplegia type 14
Homo sapiens (human)
DOID:0110766
  • hereditary spastic paraplegia 13
  • Aliases:
    • SPG13
    • autosomal dominant spastic paraplegia 13
Homo sapiens (human)
DOID:0110793
  • hereditary spastic paraplegia 41
  • Aliases:
    • SPG41
    • autosomal dominant spastic paraplegia 41
    • autosomal dominant spastic paraplegia type 41
Homo sapiens (human)
DOID:0110794
  • hereditary spastic paraplegia 42
  • Aliases:
    • SPG42
    • autosomal dominant spastic paraplegia 42
    • autosomal dominant spastic paraplegia type 42
Homo sapiens (human)
DOID:0110768
  • hereditary spastic paraplegia 15
  • Aliases:
    • Kjellin syndrome
    • SPG15
    • autosomal recessive spastic paraplegia 15
    • autosomal recessive spastic paraplegia type 15
    • hereditary spastic paraparesis type 15
    • spastic paraplegia and retinal degeneration
    • spastic paraplegia-retinal degeneration syndrome
Homo sapiens (human)
DOID:4810
  • cerebrotendinous xanthomatosis
  • Aliases:
    • Cholestanol storage disease
Homo sapiens (human)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Homo sapiens (human)
DOID:28
  • endocrine system disease
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Homo sapiens (human)
DOID:0080102
  • congenital myopathy 4A
  • Aliases:
    • CFTD
    • congenital fiber-type disproportion
Homo sapiens (human)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Homo sapiens (human)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Mus musculus (house mouse)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Rattus norvegicus (Norway rat)
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Mus musculus (house mouse)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Mus musculus (house mouse)
DOID:28
  • endocrine system disease
Mus musculus (house mouse)
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Last updated: August 19, 2024