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 3451 - 3475 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0110781
  • hereditary spastic paraplegia 30
  • Aliases:
    • SPG30
    • autosomal spastic paraplegia type 30
Homo sapiens (human)
DOID:0110780
  • hereditary spastic paraplegia 29
  • Aliases:
    • SPG29
    • autosomal dominant spastic paraplegia 29
Homo sapiens (human)
DOID:0110779
  • hereditary spastic paraplegia 28
  • Aliases:
    • SPG28
    • autosomal recessive spastic paraplegia 28
    • autosomal recessive spastic paraplegia type 28
Homo sapiens (human)
DOID:0110778
  • hereditary spastic paraplegia 27
  • Aliases:
    • SPG27
    • autosomal recessive spastic paraplegia 27
    • autosomal recessive spastic paraplegia type 27
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
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
Danio rerio (zebrafish)
DOID:0110777
  • hereditary spastic paraplegia 26
  • Aliases:
    • GM2 synthase deficiency
    • SPG26
    • autosomal recessive spastic paraplegia 26
    • autosomal recessive spastic paraplegia type 26
Xenopus laevis (African clawed frog)
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
Xenopus tropicalis (tropical clawed frog)
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:0110776
  • hereditary spastic paraplegia 25
  • Aliases:
    • SPG25
    • autosomal recessive spastic paraplegia 25
    • autosomal recessive spastic paraplegia type 25
Homo sapiens (human)
DOID:0110775
  • hereditary spastic paraplegia 24
  • Aliases:
    • SPG24
    • autosomal recessive spastic paraplegia 24
    • autosomal recessive spastic paraplegia type 24
Homo sapiens (human)
DOID:0110774
  • hereditary spastic paraplegia 23
  • Aliases:
    • Lison syndrome
    • SPG23
    • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
    • spastic paraplegia 23
    • spastic paraplegia with pigmentary abnormalities
Homo sapiens (human)
DOID:0110773
  • hereditary spastic paraplegia 2
  • Aliases:
    • SPG2
    • X-linked spastic paraplegia 2
    • spastic paraplegia type 2
Homo sapiens (human)
DOID:0110772
  • hereditary spastic paraplegia 19
  • Aliases:
    • SPG19
    • autosomal dominant spastic paraplegia 19
    • autosomal dominant spastic paraplegia type 19
Homo sapiens (human)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Homo sapiens (human)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Homo sapiens (human)
DOID:0110769
  • hereditary spastic paraplegia 16
  • Aliases:
    • SPG16
    • X-linked spastic paraplegia 16
    • X-linked spastic paraplegia type 16
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: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:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Homo sapiens (human)
DOID:0110764
  • hereditary spastic paraplegia 11
  • Aliases:
    • HSP-TCC
    • Nakamura-Osame syndrome
    • SPG11
    • autosomal recessive spastic paraplegia 11
    • autosomal recessive spastic paraplegia complicated with thin corpus callosum
    • autosomal recessive spastic paraplegia type 11
    • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
    • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
Homo sapiens (human)
DOID:0110763
  • hereditary spastic paraplegia 10
  • Aliases:
    • SPG10
    • autosomal dominant spastic paraplegia 10
    • autosomal dominant spastic paraplegia type 10
Homo sapiens (human)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Homo sapiens (human)

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