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 1351 - 1375 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0081312
  • T-cell non-Hodgkin lymphoma
Rattus norvegicus (Norway rat)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Rattus norvegicus (Norway rat)
DOID:0060108
  • brain glioma
  • Aliases:
    • lower grade glioma
Rattus norvegicus (Norway rat)
DOID:848
  • arthritis
  • Aliases:
    • Inflammatory disorder of joint
Rattus norvegicus (Norway rat)
DOID:114
  • heart disease
Rattus norvegicus (Norway rat)
DOID:0112379
  • muscular dystrophy-dystroglycanopathy type B4
  • Aliases:
    • MDDGB4
    • congenital muscular dystrophy FKTN-related
Rattus norvegicus (Norway rat)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Rattus norvegicus (Norway rat)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Rattus norvegicus (Norway rat)
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Rattus norvegicus (Norway rat)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Rattus norvegicus (Norway rat)
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Rattus norvegicus (Norway rat)
DOID:0050793
  • short QT syndrome
Rattus norvegicus (Norway rat)
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Rattus norvegicus (Norway rat)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Rattus norvegicus (Norway rat)
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Rattus norvegicus (Norway rat)
DOID:11823
  • hepatorenal syndrome
Rattus norvegicus (Norway rat)
DOID:0050741
  • alcohol dependence
  • Aliases:
    • alcoholism
Rattus norvegicus (Norway rat)
DOID:0081120
  • Graves ophthalmopathy
  • Aliases:
    • Graves orbitopathy
    • Thyroid associated ophthalmopathy
    • thyroid eye disease
Rattus norvegicus (Norway rat)
DOID:3770
  • pulmonary fibrosis
  • Aliases:
    • Fibrosis of lung
Rattus norvegicus (Norway rat)
DOID:3651
  • pyruvate carboxylase deficiency disease
  • Aliases:
    • deficiency of pyruvic carboxylase
Rattus norvegicus (Norway rat)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Rattus norvegicus (Norway rat)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Rattus norvegicus (Norway rat)
DOID:0080178
  • mucositis
Rattus norvegicus (Norway rat)
DOID:3393
  • coronary artery disease
  • Aliases:
    • CHD
    • Coronary disease
    • coronary arteriosclerosis
    • coronary heart disease
Rattus norvegicus (Norway rat)
DOID:0111910
  • spermatogenic failure
  • Aliases:
    • SPGF
Rattus norvegicus (Norway rat)

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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