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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 4851 - 4875 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:28
  • endocrine system disease
Homo sapiens (human)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Homo sapiens (human)
DOID:4810
  • cerebrotendinous xanthomatosis
  • Aliases:
    • Cholestanol storage disease
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:0080067
  • Charcot-Marie-Tooth disease type 5
  • Aliases:
    • hereditary motor and sensory neuropathy with pyramidal features
Homo sapiens (human)
DOID:0110782
  • hereditary spastic paraplegia 31
  • Aliases:
    • SPG31
    • autosomal dominant spastic paraplegia 31
    • autosomal dominant spastic paraplegia type 31
Homo sapiens (human)
DOID:0110781
  • hereditary spastic paraplegia 30
  • Aliases:
    • SPG30
    • autosomal spastic paraplegia type 30
Homo sapiens (human)
DOID:0110796
  • hereditary spastic paraplegia 44
  • Aliases:
    • SPG44
    • autosomal recessive spastic paraplegia 44
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:0110772
  • hereditary spastic paraplegia 19
  • Aliases:
    • SPG19
    • autosomal dominant spastic paraplegia 19
    • autosomal dominant spastic paraplegia type 19
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:0110815
  • hereditary spastic paraplegia 64
  • Aliases:
    • SPG64
    • autosomal recessive spastic paraplegia 64
    • autosomal recessive spastic paraplegia type 64
Homo sapiens (human)
DOID:0110789
  • hereditary spastic paraplegia 38
  • Aliases:
    • SPG38
    • autosomal dominant spastic paraplegia 38
    • autosomal dominant spastic paraplegia type 38
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:0110812
  • hereditary spastic paraplegia 61
  • Aliases:
    • SPG61
    • autosomal recessive spastic paraplegia 61
    • autosomal recessive spastic paraplegia type 61
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:0060245
  • Mast syndrome
  • Aliases:
    • SPG21
    • autosomal recessive spastic paraplegia 21
    • autosomal recessive spastic paraplegia type 21
    • hereditary spastic paraplegia 21
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:0110785
  • hereditary spastic paraplegia 34
  • Aliases:
    • SPG34
    • X-linked spastic paraplegia 34
    • X-linked spastic paraplegia type 34
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:0110783
  • hereditary spastic paraplegia 32
  • Aliases:
    • SPG32
    • autosomal recessive spastic paraplegia 32
    • autosomal recessive spastic paraplegia type 32
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: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:0110814
  • hereditary spastic paraplegia 63
  • Aliases:
    • SPG63
    • autosomal recessive spastic paraplegia 63
    • spastic paraplegia 63
Homo sapiens (human)
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Last updated: August 19, 2024