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GlyCosmos Diseases

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

Source Last Updated
Alliance of Genome Resources July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3426 - 3450 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
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)
DOID:0110805
  • hereditary spastic paraplegia 53
  • Aliases:
    • SPG53
    • autosomal recessive spastic paraplegia 53
    • autosomal recessive spastic paraplegia type 53
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:0110800
  • hereditary spastic paraplegia 48
  • Aliases:
    • SPG48
    • autosomal recessive spastic paraplegia 48
    • autosomal recessive spastic paraplegia type 48
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:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Drosophila melanogaster (fruit fly)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Mus musculus (house mouse)
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:0110796
  • hereditary spastic paraplegia 44
  • Aliases:
    • SPG44
    • autosomal recessive spastic paraplegia 44
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:0110794
  • hereditary spastic paraplegia 42
  • Aliases:
    • SPG42
    • autosomal dominant spastic paraplegia 42
    • autosomal dominant spastic paraplegia type 42
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:0110792
  • hereditary spastic paraplegia 4
  • Aliases:
    • SPG4
    • autosomal dominant spastic paraplegia 4
    • autosomal dominant spastic paraplegia type 4
Homo sapiens (human)
DOID:0110791
  • hereditary spastic paraplegia 3A
  • Aliases:
    • FSP1
    • SPG3A
    • autosomal dominant familial spastic paraplegia 1
    • autosomal dominant spastic paraplegia 3
    • autosomal dominant spastic paraplegia type 3
    • strumpell disease
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:0110789
  • hereditary spastic paraplegia 38
  • Aliases:
    • SPG38
    • autosomal dominant spastic paraplegia 38
    • autosomal dominant spastic paraplegia type 38
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:0110787
  • hereditary spastic paraplegia 36
  • Aliases:
    • SPG36
    • autosomal dominant spastic paraplegia 36
    • autosomal dominant spastic paraplegia type 36
Homo sapiens (human)
DOID:0110786
  • hereditary spastic paraplegia 35
  • Aliases:
    • FAHN
    • SPG35
    • autosomal recessive spastic paraplegia 35
    • autosomal recessive spastic paraplegia type 35
    • fatty acid hydroxylase-associated neurodegeneration
    • leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
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:0110783
  • hereditary spastic paraplegia 32
  • Aliases:
    • SPG32
    • autosomal recessive spastic paraplegia 32
    • autosomal recessive spastic paraplegia type 32
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)
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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024