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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 5701 - 5725 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:8771
  • contagious pustular dermatitis
  • Aliases:
    • Ecthyma contagiosum
    • Ecthyma, Contagious
    • Orf
    • scabby mouth
    • sheep pox
    • thistle disease
Homo sapiens (human)
DOID:8743
  • erythema infectiosum
  • Aliases:
    • Fifth disease
Homo sapiens (human)
DOID:8736
  • smallpox
  • Aliases:
    • Ordinary smallpox
Homo sapiens (human)
DOID:8956
  • cowpox
  • Aliases:
    • yaba
Homo sapiens (human)
DOID:9153
  • variola minor
  • Aliases:
    • Alastrim
    • cottonpox
    • milkpox
    • whitepox
Homo sapiens (human)
DOID:0060123
  • connective tissue benign neoplasm
  • Aliases:
    • mesenchymal tissue neoplasm
    • neoplasm of soft tissue
    • neoplasm of soft tissues
    • soft tissue benign neoplasm
    • tumor of the soft tissue
Homo sapiens (human)
DOID:0050562
  • West syndrome
Homo sapiens (human)
DOID:2481
  • obsolete infantile epileptic encephalopathy
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Homo sapiens (human)
DOID:0080067
  • Charcot-Marie-Tooth disease type 5
  • Aliases:
    • hereditary motor and sensory neuropathy with pyramidal features
Homo sapiens (human)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
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:0110773
  • hereditary spastic paraplegia 2
  • Aliases:
    • SPG2
    • X-linked spastic paraplegia 2
    • spastic paraplegia type 2
Homo sapiens (human)
DOID:0110816
  • hereditary spastic paraplegia 7
  • Aliases:
    • SPG7
    • autosomal recessive spastic paraplegia 7
    • spastic paraplegia type 7
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:0110763
  • hereditary spastic paraplegia 10
  • Aliases:
    • SPG10
    • autosomal dominant spastic paraplegia 10
    • autosomal dominant spastic paraplegia type 10
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: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:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
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:0110808
  • hereditary spastic paraplegia 56
  • Aliases:
    • SPG56
    • autosomal recessive spastic paraplegia 56
    • autosomal recessive spastic paraplegia type 56
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:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
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)
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Last updated: August 19, 2024