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 5501 - 5525 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0070432
  • hyperphosphatasia with impaired intellectual development syndrome 5
  • Aliases:
    • GPIBD11
    • HPMRS5
    • glycosylphosphatidylinositol biosynthesis defect 11
    • hyperphosphatasia with mental retardation syndrome 5
Homo sapiens (human)
DOID:0060227
  • Adams-Oliver syndrome
  • Aliases:
    • Adams Oliver syndrome
Homo sapiens (human)
DOID:0050441
  • mucosulfatidosis
  • Aliases:
    • Sulfatidosis, Juvenile, Austin Type
    • multiple sulfatase deficiency disease
Homo sapiens (human)
DOID:13272
  • Klebsiella pneumonia
  • Aliases:
    • Pneumonia due to Klebsiella pneumoniae
    • Pneumonia due to Klebsiella pneumoniae (disorder)
Homo sapiens (human)
DOID:7371
  • superficial urinary bladder cancer
  • Aliases:
    • Superficial urinary bladder carcinoma
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:7941
  • Barrett's adenocarcinoma
  • Aliases:
    • Barrett adenocarcinoma
    • adenocarcinoma Arising in Barrett's Mucosa
Homo sapiens (human)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Homo sapiens (human)
DOID:14701
  • propionic acidemia
  • Aliases:
    • GLYCINEMIA, KETOTIC
    • KETOTIC HYPERGLYCINEMIA
    • ketotic II glycinemia
    • ketotic glycinemia
    • propionic aciduria
    • propionyl-CoA carboxylase deficiency
Homo sapiens (human)
DOID:0110406
  • retinitis pigmentosa 30
  • Aliases:
    • RP30
Homo sapiens (human)
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Homo sapiens (human)
DOID:10590
  • mild pre-eclampsia
Homo sapiens (human)
DOID:0080556
  • congenital disorder of glycosylation Id
  • Aliases:
    • congenital disorder of glycosylation 1d
Rattus norvegicus (Norway rat)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Rattus norvegicus (Norway rat)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Rattus norvegicus (Norway rat)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Rattus norvegicus (Norway rat)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Rattus norvegicus (Norway rat)
DOID:0111230
  • congenital muscular dystrophy-dystroglycanopathy type A11
  • Aliases:
    • MDDGA11
    • Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
Rattus norvegicus (Norway rat)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Rattus norvegicus (Norway rat)
DOID:0050571
  • congenital disorder of glycosylation type II
Rattus norvegicus (Norway rat)
DOID:0050967
  • spinocerebellar ataxia type 17
Homo sapiens (human)
DOID:0080998
  • acute necrotizing pancreatitis
Rattus norvegicus (Norway rat)
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Rattus norvegicus (Norway rat)

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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