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 2251 - 2275 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:533
  • thymus gland disease
  • Aliases:
    • disease of thymus gland
Homo sapiens (human)
DOID:12583
  • velocardiofacial syndrome
  • Aliases:
    • Shprintzen syndrome
    • VCF-Velocardiofacial syndrome
Homo sapiens (human)
DOID:6951
  • telangiectatic osteogenic sarcoma
  • Aliases:
    • Telangiectatic osteosarcoma
Homo sapiens (human)
DOID:2018
  • hyperinsulinism
  • Aliases:
    • hyperinsulinemia
Homo sapiens (human)
DOID:8931
  • Evans' syndrome
Homo sapiens (human)
DOID:7633
  • macular holes
  • Aliases:
    • Macular hole
Homo sapiens (human)
DOID:11502
  • mitral valve insufficiency
  • Aliases:
    • Congenital insufficiency of mitral valve
    • Mitral valve incompetence
    • congenital mitral insufficiency
    • congenital mitral regurgitation
    • mitral regurgitation
Homo sapiens (human)
DOID:583
  • hemolytic anemia
  • Aliases:
    • ANEMIA HEMOLYTIC
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:11527
  • laryngostenosis
  • Aliases:
    • Stenosis of larynx
Homo sapiens (human)
DOID:0080162
  • lupus nephritis
Homo sapiens (human)
DOID:0050811
  • congenital adrenal hyperplasia
  • Aliases:
    • adrenal hyperplasia 1
    • congenital lipoid adrenal hyperplasia
    • lipoid CAH
Homo sapiens (human)
DOID:0070313
  • thiamine deficiency disease
Homo sapiens (human)
DOID:0070133
  • autosomal recessive cutis laxa type IB
  • Aliases:
    • ARCL1B
Homo sapiens (human)
DOID:0111225
  • centronuclear myopathy X-linked
  • Aliases:
    • CNMX
    • MTM1
    • X-linked myotubular myopathy
    • XLCNM
    • XLMTM
    • myotubular myopathy 1
Homo sapiens (human)
DOID:0111228
  • Sveinsson chorioretinal atrophy
  • Aliases:
    • HPCD
    • SCRA
    • atrophia areata
    • helicoid peripapillary chorioretinal degeneration
    • peripapillary chorioretinal degeneration, Icelandic type
Homo sapiens (human)
DOID:10602
  • obsolete steatorrhea
Homo sapiens (human)
DOID:0110736
  • neurodegeneration with brain iron accumulation 2b
  • Aliases:
    • NBIA2b
    • Neuroaxonal Dystrophy, Atypical
    • Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related
Homo sapiens (human)
DOID:3087
  • gingivitis
  • Aliases:
    • acute gingivitis
    • chronic gingivitis
Homo sapiens (human)
DOID:0110106
  • atrial heart septal defect 1
  • Aliases:
    • ASD1
    • atrial septal defect 1
Homo sapiens (human)
DOID:3717
  • gastric adenocarcinoma
  • Aliases:
    • adenocarcinoma of stomach
    • stomach adenocarcinoma
Homo sapiens (human)
DOID:13328
  • diabetic cataract
  • Aliases:
    • Cataract - diabetic
Homo sapiens (human)
DOID:3753
  • Hermansky-Pudlak syndrome
Homo sapiens (human)
DOID:11355
  • bladder calculus
Homo sapiens (human)
DOID:5509
  • childhood ependymoma
Homo sapiens (human)

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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