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 5151 - 5175 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:5572
  • Beckwith-Wiedemann syndrome
Homo sapiens (human)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Homo sapiens (human)
DOID:484
  • vascular hemostatic disease
Homo sapiens (human)
DOID:5495
  • monophasic synovial sarcoma
  • Aliases:
    • Monophasic sarcoma of Synovium
Homo sapiens (human)
DOID:0090048
  • dystonia 16
Homo sapiens (human)
DOID:2632
  • papillary serous adenocarcinoma
  • Aliases:
    • Micropapillary serous carcinoma
    • Papillary serous carcinoma
    • serous surface papillary carcinoma
Homo sapiens (human)
DOID:635
  • acquired immunodeficiency syndrome
  • Aliases:
    • AIDS
    • acquired Immune deficiency
Homo sapiens (human)
DOID:417
  • autoimmune disease
  • Aliases:
    • autoimmune hypersensitivity disease
    • hypersensitivity reaction type II disease
Homo sapiens (human)
DOID:0060067
  • Pearson syndrome
  • Aliases:
    • Pearson Marrow-Pancreas Syndrome
Homo sapiens (human)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Homo sapiens (human)
DOID:10138
  • xerophthalmia
  • Aliases:
    • Conjunctival xerosis
Homo sapiens (human)
DOID:2691
  • myoma
  • Aliases:
    • benign neoplasm of the Muscle
Homo sapiens (human)
DOID:4953
  • poliomyelitis
Homo sapiens (human)
DOID:1580
  • diffuse scleroderma
  • Aliases:
    • diffuse systemic sclerosis
    • systemic sclerosis, diffuse
Homo sapiens (human)
DOID:0110170
  • Charcot-Marie-Tooth disease axonal type 2Q
  • Aliases:
    • CMT2Q
    • Charcot-Marie-Tooth neuropathy type 2Q
    • autosomal dominant Charcot-Marie-Tooth disease type 2Q
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
Homo sapiens (human)
DOID:0110460
  • dilated cardiomyopathy 2A
  • Aliases:
    • CMD2A
Homo sapiens (human)
DOID:0090092
  • hypogonadotropic hypogonadism 3 with or without anosmia
Homo sapiens (human)
DOID:0060316
  • orofaciodigital syndrome I
  • Aliases:
    • Papillon-Leage-Psaume syndrome
    • orofaciodigital syndrome 1
    • orofaciodigital syndrome type I
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
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:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Homo sapiens (human)
DOID:0081337
  • congenital myopathy
Homo sapiens (human)
DOID:14789
  • spondyloepiphyseal dysplasia congenita
  • Aliases:
    • Late Spondyloepiphyseal Dysplasia
Homo sapiens (human)
DOID:4404
  • occupational dermatitis
  • Aliases:
    • Occupational allergic contact dermatitis
    • Occupational eczema
Homo sapiens (human)
DOID:12798
  • mucopolysaccharidosis
Homo sapiens (human)

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Last updated: August 19, 2024