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 4001 - 4025 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0060535
  • Warsaw breakage syndrome
  • Aliases:
    • WABS
Homo sapiens (human)
DOID:0110719
  • Warburg micro syndrome 4
  • Aliases:
    • Micro Syndrome 4
    • WARBM4
Homo sapiens (human)
DOID:0110718
  • Warburg micro syndrome 3
  • Aliases:
    • Micro Syndrome 3
    • WARBM3
Homo sapiens (human)
DOID:0110717
  • Warburg micro syndrome 2
  • Aliases:
    • Micro Syndrome 2
    • WARBM2
Homo sapiens (human)
DOID:0110716
  • Warburg micro syndrome 1
  • Aliases:
    • Micro Syndrome 1
    • WARBM1
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Homo sapiens (human)
DOID:9258
  • Waardenburg syndrome
  • Aliases:
    • Waardenburg Shah syndrome
    • Waardenburg's syndrome
    • van der Hoeve Halbertsona Waardenburg syndrome
Homo sapiens (human)
DOID:0110949
  • Waardenburg syndrome type 3
  • Aliases:
    • Klein-Waardenburg syndrome
    • WS3
    • Waardenburg syndrome type III
    • Waardenburg syndrome with upper limb anomalies
Homo sapiens (human)
DOID:0110948
  • Waardenburg syndrome type 1
  • Aliases:
    • WS1
    • Waardenburg syndrome type I
Homo sapiens (human)
DOID:14515
  • WAGR syndrome
  • Aliases:
    • 11p partial monosomy syndrome
    • Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome
    • chromosome 11p13 deletion syndrome
Homo sapiens (human)
DOID:12297
  • Vogt-Koyanagi-Harada disease
  • Aliases:
    • Harada's disease
    • Vogt-Koyanagi syndrome
    • uveomeningoencephalitic syndrome
Homo sapiens (human)
DOID:9584
  • Venezuelan equine encephalitis
Homo sapiens (human)
DOID:0060239
  • Van der Woude syndrome
Homo sapiens (human)
DOID:5574
  • VIPoma
  • Aliases:
    • VIP- Secreting tumor
    • Vasoactive intestinal peptide-secreting tumor
    • Vipoma, malignant
    • malignant vasoactive intestinal peptide-secreting tumor
Homo sapiens (human)
DOID:14679
  • VACTERL association
Homo sapiens (human)
DOID:0050439
  • Usher syndrome
Homo sapiens (human)
DOID:0110841
  • Usher syndrome type 3A
  • Aliases:
    • USH3A
    • Usher syndrome type IIIA
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:3535
  • Unverricht-Lundborg syndrome
  • Aliases:
    • Unverricht - Lundborg disease
    • Unverricht's disease
    • Unverricht-Lundborg disease
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Homo sapiens (human)
DOID:3491
  • Turner syndrome
  • Aliases:
    • Bonnevie-Ullrich syndrome
    • Gonadal dysgenesis - Turner
    • Karyotype 45, X
    • Monosomy X
    • XO syndrome
    • monosomy X syndrome
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:2908
  • Treacher Collins syndrome
  • Aliases:
    • Franceschetti syndrome
    • mandibulofacial dysostosis
Homo sapiens (human)

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Last updated: August 19, 2024