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 2926 - 2950 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:4677
  • keratitis
Drosophila melanogaster (fruit fly)
DOID:0060911
  • karyomegalic interstitial nephritis
  • Aliases:
    • KIN
    • KMIN
Homo sapiens (human)
DOID:12376
  • juvenile spinal muscular atrophy
  • Aliases:
    • Kugelberg-Welander disease
    • SMA3
    • Spinal Muscular Atrophy Type 3
    • Type III Spinal Muscular Atrophy
Homo sapiens (human)
DOID:676
  • juvenile rheumatoid arthritis
  • Aliases:
    • Pauciarticular onset juvenile chronic arthritis
    • Still's disease
    • acute juvenile rheumatoid arthritis
    • juvenile chronic polyarthritis
    • juvenile idiopathic arthritis
    • monarticular juvenile rheumatoid arthritis
    • pauciarticular juvenile arthritis
    • systemic juvenile rheumatoid arthritis
Homo sapiens (human)
DOID:676
  • juvenile rheumatoid arthritis
  • Aliases:
    • Pauciarticular onset juvenile chronic arthritis
    • Still's disease
    • acute juvenile rheumatoid arthritis
    • juvenile chronic polyarthritis
    • juvenile idiopathic arthritis
    • monarticular juvenile rheumatoid arthritis
    • pauciarticular juvenile arthritis
    • systemic juvenile rheumatoid arthritis
Mus musculus (house mouse)
DOID:0050787
  • juvenile polyposis syndrome
Homo sapiens (human)
DOID:6811
  • juvenile pilocytic astrocytoma
Homo sapiens (human)
DOID:4890
  • juvenile myoclonic epilepsy
Homo sapiens (human)
DOID:0050458
  • juvenile myelomonocytic leukemia
Homo sapiens (human)
DOID:1068
  • juvenile glaucoma
  • Aliases:
    • Glaucoma of childhood
Homo sapiens (human)
DOID:0081381
  • juvenile amyotrophic lateral sclerosis type 27
Homo sapiens (human)
DOID:3209
  • junctional epidermolysis bullosa
  • Aliases:
    • congenital junctional epidermolysis bullosa
Homo sapiens (human)
DOID:0060733
  • junctional epidermolysis bullosa with pyloric atresia
  • Aliases:
    • Carmi syndrome
    • JEB-PA
    • epidermolysis bullosa junctionalis with pyloric atresia
    • junctional epidermolysis bullosa-pyloric atresia syndrome
Homo sapiens (human)
DOID:0060738
  • junctional epidermolysis bullosa non-Herlitz type
  • Aliases:
    • GABEB
    • JEB-nH gen
    • JEN-nH
    • generalized atrophic benign epidermolysis bullosa
    • generalized junctional epidermolysis bullosa, non-Herlitz type
    • junctional epidermolysis bullosa generalisata mitis
    • junctional epidermolysis bullosa, Disentis type
Homo sapiens (human)
DOID:0060188
  • jejunoileitis
Homo sapiens (human)
DOID:14753
  • isovaleric acidemia
  • Aliases:
    • Isovaleryl-CoA dehydrogenase deficiency
    • isovaleric acid CoA dehydrogenase deficiency
    • isovaleric aciduria
Homo sapiens (human)
DOID:0060841
  • isolated microphthalmia 8
  • Aliases:
    • MCOP8
Homo sapiens (human)
DOID:0060838
  • isolated microphthalmia 7
  • Aliases:
    • MCOP7
Homo sapiens (human)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Homo sapiens (human)
DOID:0060836
  • isolated microphthalmia 4
  • Aliases:
    • MCOP4
Homo sapiens (human)
DOID:0060842
  • isolated microphthalmia 3
  • Aliases:
    • MCOP3
Homo sapiens (human)
DOID:0060839
  • isolated microphthalmia 2
  • Aliases:
    • MCOP2
Homo sapiens (human)
DOID:0060840
  • isolated microphthalmia 1
  • Aliases:
    • MCOP1
Homo sapiens (human)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Homo sapiens (human)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)

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Last updated: August 19, 2024