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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 3051 - 3075 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0110783
  • hereditary spastic paraplegia 32
  • Aliases:
    • SPG32
    • autosomal recessive spastic paraplegia 32
    • autosomal recessive spastic paraplegia type 32
Homo sapiens (human)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
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:0110776
  • hereditary spastic paraplegia 25
  • Aliases:
    • SPG25
    • autosomal recessive spastic paraplegia 25
    • autosomal recessive spastic paraplegia type 25
Homo sapiens (human)
DOID:0110781
  • hereditary spastic paraplegia 30
  • Aliases:
    • SPG30
    • autosomal spastic paraplegia type 30
Homo sapiens (human)
DOID:0110814
  • hereditary spastic paraplegia 63
  • Aliases:
    • SPG63
    • autosomal recessive spastic paraplegia 63
    • spastic paraplegia 63
Homo sapiens (human)
DOID:0110797
  • hereditary spastic paraplegia 45
  • Aliases:
    • SPG45
    • SPG65
    • autosomal recessive spastic paraplegia 45
    • autosomal recessive spastic paraplegia type 45
    • autosomal recessive spastic paraplegia type 65
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:0110824
  • hereditary spastic paraplegia 9A
  • Aliases:
    • AD-SPG9A
    • Cataracts motor neuropathy-short stature-skeletal anomalies syndrome
    • SPG9A
    • autosomal dominant complex spastic paraplegia type 9A
    • autosomal dominant spastic paraplegia 9A
    • cataracts with motor neuronopathy, short stature and skeletal abnormalities
    • spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
    • spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
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:0110773
  • hereditary spastic paraplegia 2
  • Aliases:
    • SPG2
    • X-linked spastic paraplegia 2
    • spastic paraplegia type 2
Homo sapiens (human)
DOID:0110807
  • hereditary spastic paraplegia 55
  • Aliases:
    • SPG55
    • autosomal recessive spastic paraplegia 55
    • autosomal recessive spastic paraplegia type 55
Homo sapiens (human)
DOID:0110800
  • hereditary spastic paraplegia 48
  • Aliases:
    • SPG48
    • autosomal recessive spastic paraplegia 48
    • autosomal recessive spastic paraplegia type 48
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:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Homo sapiens (human)
DOID:0110788
  • hereditary spastic paraplegia 37
  • Aliases:
    • SPG37
    • autosomal dominant spastic paraplegia 37
    • autosomal dominant spastic paraplegia type 37
Homo sapiens (human)
DOID:0060491
  • SPOAN syndrome
  • Aliases:
    • spastic paraplegia, optic atropy, and neuropathy
    • spastic paraplegia, optic atropy, and neuropathy syndrome
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:0110805
  • hereditary spastic paraplegia 53
  • Aliases:
    • SPG53
    • autosomal recessive spastic paraplegia 53
    • autosomal recessive spastic paraplegia type 53
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:0110801
  • hereditary spastic paraplegia 49
  • Aliases:
    • SPG49
    • autosomal recessive spastic paraplegia 49
    • autosomal recessive spastic paraplegia type 49
Homo sapiens (human)
DOID:0110790
  • hereditary spastic paraplegia 39
  • Aliases:
    • NTE-related motor neuron disorder
    • NTEMND
    • SPG39
    • autosomal recessive spastic paraplegia 39
    • autosomal recessive spastic paraplegia type 39
    • spastic paraplegia due to NTE mutation
    • spastic paraplegia due to neuropathy target esterase mutation
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:0110780
  • hereditary spastic paraplegia 29
  • Aliases:
    • SPG29
    • autosomal dominant spastic paraplegia 29
Homo sapiens (human)
DOID:0110806
  • hereditary spastic paraplegia 54
  • Aliases:
    • SPG54
    • autosomal recessive spastic paraplegia 54
    • autosomal recessive spastic paraplegia type 54
Homo sapiens (human)
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Last updated: August 19, 2024