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 5226 - 5250 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0110844
  • xeroderma pigmentosum group C
  • Aliases:
    • XP group C
    • XP3
    • XPC
    • XPCC
    • xeroderma pigmentosum III
Homo sapiens (human)
DOID:0110843
  • xeroderma pigmentosum group A
  • Aliases:
    • XP group A
    • XP1
    • XPA
    • xeroderma pigmentosum 1
    • xeroderma pigmentosum complementation group A
Homo sapiens (human)
DOID:0110841
  • Usher syndrome type 3A
  • Aliases:
    • USH3A
    • Usher syndrome type IIIA
Homo sapiens (human)
DOID:0110829
  • retinitis pigmentosa-deafness syndrome
Homo sapiens (human)
DOID:0110828
  • Usher syndrome type 3
  • Aliases:
    • USH3
Homo sapiens (human)
DOID:0110827
  • Usher syndrome type 2
  • Aliases:
    • USH2
Homo sapiens (human)
DOID:0110826
  • Usher syndrome type 1
  • Aliases:
    • US1
    • USH1
Homo sapiens (human)
DOID:0110825
  • hereditary spastic paraplegia 9B
  • Aliases:
    • SPG9B
    • autosomal recessive complex spastic paraplegia type 9B
    • autosomal recessive spastic paraplegia 9B
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:0110823
  • hereditary spastic paraplegia 8
  • Aliases:
    • SPG8
    • autosomal dominant spastic paraplegia 8
    • autosomal dominant spastic paraplegia type 8
Homo sapiens (human)
DOID:0110822
  • hereditary spastic paraplegia 77
  • Aliases:
    • SPG77
    • autosomal recessive spastic paraplegia 77
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:0110818
  • hereditary spastic paraplegia 73
  • Aliases:
    • SPG73
    • autosomal dominant spastic paraplegia 73
    • autosomal dominant spastic paraplegia type 73
Homo sapiens (human)
DOID:0110817
  • hereditary spastic paraplegia 72A
  • Aliases:
    • SPG72
    • autosomal spastic paraplegia type 72
Homo sapiens (human)
DOID:0110816
  • hereditary spastic paraplegia 7
  • Aliases:
    • SPG7
    • autosomal recessive spastic paraplegia 7
    • spastic paraplegia type 7
Homo sapiens (human)
DOID:0110815
  • hereditary spastic paraplegia 64
  • Aliases:
    • SPG64
    • autosomal recessive spastic paraplegia 64
    • autosomal recessive spastic paraplegia type 64
Homo sapiens (human)
DOID:0110814
  • hereditary spastic paraplegia 63
  • Aliases:
    • SPG63
    • autosomal recessive spastic paraplegia 63
    • spastic paraplegia 63
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:0110812
  • hereditary spastic paraplegia 61
  • Aliases:
    • SPG61
    • autosomal recessive spastic paraplegia 61
    • autosomal recessive spastic paraplegia type 61
Homo sapiens (human)
DOID:0110811
  • hereditary spastic paraplegia 6
  • Aliases:
    • FSP3
    • SPG6
    • autosomal dominant familial spastic paraplegia type 3
    • autosomal dominant spastic paraplegia 6
    • autosomal dominant spastic paraplegia type 6
Homo sapiens (human)
DOID:0110810
  • hereditary spastic paraplegia 5A
  • Aliases:
    • SPG5A
    • autosomal recessive spastic paraplegia 5A
    • autosomal recessive spastic paraplegia type 5A
Homo sapiens (human)
DOID:0110809
  • hereditary spastic paraplegia 57
  • Aliases:
    • SPG57
    • autosomal recessive spastic paraplegia 57
    • autosomal recessive spastic paraplegia type 57
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:0110807
  • hereditary spastic paraplegia 55
  • Aliases:
    • SPG55
    • autosomal recessive spastic paraplegia 55
    • autosomal recessive spastic paraplegia type 55
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