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 276 - 300 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:11550
  • oculomotor nerve paralysis
  • Aliases:
    • III nerve palsy
    • IIIrd nerve Paralysis
    • Third cranial nerve paralysis
Homo sapiens (human)
DOID:0110016
  • Leber congenital amaurosis 2
  • Aliases:
    • LCA2
    • amaurosis congenita of Leber II
Homo sapiens (human)
DOID:0090114
  • Sorsby's fundus dystrophy
  • Aliases:
    • SFD
    • hemorrhagic macular dystrophy
    • pseudoinflammatory fundus dystrophy of Sorsby
Homo sapiens (human)
DOID:0060745
  • Doyne honeycomb retinal dystrophy
  • Aliases:
    • DHRD
    • Doyne honeycomb degeneration of retina
Homo sapiens (human)
DOID:8465
  • retinoschisis
Homo sapiens (human)
DOID:12165
  • retinal lattice degeneration
  • Aliases:
    • Palisade degeneration of retina
Homo sapiens (human)
DOID:0060746
  • basal laminar drusen
  • Aliases:
    • cuticular drusen
    • drusen of bruch membrane
    • early adult-onset grouped drusen
Homo sapiens (human)
DOID:9821
  • choroideremia
  • Aliases:
    • progressive Choroidal Atrophy
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:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:0050882
  • spinocerebellar ataxia type 5
Homo sapiens (human)
DOID:0110384
  • retinitis pigmentosa 25
  • Aliases:
    • RP25
Homo sapiens (human)
DOID:0112343
  • hereditary spastic paraplegia 82
  • Aliases:
    • SPG82
    • spastic paraplegia 82 autosomal recessive
Homo sapiens (human)
DOID:0070264
  • congenital disorder of glycosylation type IIl
  • Aliases:
    • CDG IIl
    • CDG syndrome type IIL
    • CDG2L
    • CDGIIdl
    • COG6-CGD
    • Congenital disorder of glycosylation type 2l
Homo sapiens (human)
DOID:0060230
  • basal ganglia calcification
  • Aliases:
    • Fahr disease
Homo sapiens (human)
DOID:4514
  • thyroid angiosarcoma
  • Aliases:
    • hemangiosarcoma of the Thyroid
Homo sapiens (human)
DOID:0080822
  • aspirin-induced respiratory disease
  • Aliases:
    • aspirin-sensitive asthma
Homo sapiens (human)
DOID:9946
  • steroid-induced glaucoma
  • Aliases:
    • Corticosteroid-induced glaucoma
Homo sapiens (human)
DOID:7519
  • endocervical carcinoma
  • Aliases:
    • carcinoma of endocervix
    • carcinoma of the Endocervix
Homo sapiens (human)
DOID:0111167
  • Dyggve-Melchior-Clausen disease
  • Aliases:
    • DMC disease
    • pseudo-Morquio disease type I
Homo sapiens (human)
DOID:12237
  • bile reflux
Homo sapiens (human)
DOID:0080160
  • Cytomegalovirus retinitis
  • Aliases:
    • CMV retinitis
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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