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 451 - 475 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:7134
  • esophagus small cell carcinoma
  • Aliases:
    • Oat cell carcinoma of esophagus
    • Oat cell carcinoma of oesophagus
    • oesophagus small cell carcinoma
Homo sapiens (human)
DOID:6901
  • familiar ovarian carcinoma
Homo sapiens (human)
DOID:0050690
  • brachyolmia
  • Aliases:
    • brachyrachia
Homo sapiens (human)
DOID:0050812
  • spondyloepimetaphyseal dysplasia, Pakistani type
  • Aliases:
    • spondyloepimetaphyseal dysplasia Pakistani type
Homo sapiens (human)
DOID:0112237
  • lissencephaly 1
  • Aliases:
    • LIS1
    • PAFAH1B1-related lissencephaly
Homo sapiens (human)
DOID:0060432
  • chromosome 17p13.3 duplication syndrome
  • Aliases:
    • 17p13.3 duplication syndrome
    • 17p13.3 microduplication syndrome
    • chromosome 17p13.3 centromeric duplication syndrome
    • trisomy 17p13.3
Homo sapiens (human)
DOID:0110403
  • retinitis pigmentosa 13
  • Aliases:
    • RP13
Homo sapiens (human)
DOID:0060763
  • X-linked juvenile retinoschisis 1
  • Aliases:
    • X-linked juvenile retinoschisis
    • X-linked retinoschisis
    • XLRS
Homo sapiens (human)
DOID:11427
  • endosalpingiosis
Homo sapiens (human)
DOID:3437
  • laryngitis
Homo sapiens (human)
DOID:10290
  • prostate lymphoma
  • Aliases:
    • lymphoma of prostate
Homo sapiens (human)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Homo sapiens (human)
DOID:2661
  • myoepithelioma
  • Aliases:
    • Myoepithelial adenoma
    • Myoepithelial neoplasm
    • benign myoepithelioma
Homo sapiens (human)
DOID:6933
  • bladder transitional cell papilloma
  • Aliases:
    • Urothelial papilloma
    • bladder papilloma
    • transitional cell papilloma of bladder
    • urinary bladder Urothelial papilloma
Homo sapiens (human)
DOID:6217
  • gastric diffuse adenocarcinoma
Homo sapiens (human)
DOID:0070468
  • Yoon-Bellen neurodevelopmental syndrome
  • Aliases:
    • YOBELN
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Homo sapiens (human)
DOID:0110008
  • achromatopsia 3
  • Aliases:
    • ACHM1
    • ACHM3
    • Pingelapese blindness
    • RMCH1
    • rod monochromacy 1
    • rod monochromatism 1
Homo sapiens (human)
DOID:0110865
  • congenital stationary night blindness 1B
  • Aliases:
    • CSNB1B
    • autosomal recessive complete congenital stationary night blindness
    • congenital stationary night blindness 1B autosomal recessive
Homo sapiens (human)
DOID:0110871
  • congenital stationary night blindness 2A
  • Aliases:
    • congenital stationary night blindness 2A X-linked
Homo sapiens (human)
DOID:0090059
  • enhanced S-cone syndrome
Homo sapiens (human)
DOID:4692
  • endophthalmitis
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:0080325
  • tuberous sclerosis 2
Homo sapiens (human)
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
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