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 3201 - 3225 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0112250
  • Gaucher's disease type IIIC
  • Aliases:
    • GD3C
    • Gaucher disease type 3C
    • Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
    • Gaucher-like disease
    • cardiovascular Gaucher disease
Caenorhabditis elegans
DOID:0112250
  • Gaucher's disease type IIIC
  • Aliases:
    • GD3C
    • Gaucher disease type 3C
    • Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
    • Gaucher-like disease
    • cardiovascular Gaucher disease
Mus musculus (house mouse)
DOID:0112250
  • Gaucher's disease type IIIC
  • Aliases:
    • GD3C
    • Gaucher disease type 3C
    • Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
    • Gaucher-like disease
    • cardiovascular Gaucher disease
Homo sapiens (human)
DOID:0112251
  • Ghosal hematodiaphyseal syndrome
  • Aliases:
    • Ghosal hematodiaphyseal dysplasia
    • Ghosal syndrome
    • diaphyseal dysplasia-anemia syndrome
Homo sapiens (human)
DOID:0112263
  • hypoinsulinemic hypoglycemia with hemihypertrophy
  • Aliases:
    • HIHGHH
    • hypoinsulinemic hypoglycemia and body hemihypertrophy
Mus musculus (house mouse)
DOID:0112263
  • hypoinsulinemic hypoglycemia with hemihypertrophy
  • Aliases:
    • HIHGHH
    • hypoinsulinemic hypoglycemia and body hemihypertrophy
Homo sapiens (human)
DOID:0112263
  • hypoinsulinemic hypoglycemia with hemihypertrophy
  • Aliases:
    • HIHGHH
    • hypoinsulinemic hypoglycemia and body hemihypertrophy
Rattus norvegicus (Norway rat)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Xenopus tropicalis (tropical clawed frog)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Homo sapiens (human)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Homo sapiens (human)
DOID:0112298
  • spondylometaphyseal dysplasia Sedaghatian type
  • Aliases:
    • SMDS
    • Sedaghatian chondrodysplasia
    • congenital lethal metaphyseal chondrodysplasia
Saccharomyces cerevisiae S288C
DOID:0112300
  • spondylometaphyseal dysplasia with cone-rod dystrophy
  • Aliases:
    • SMD-CRD
    • SMDCRD
    • spondylometaphyseal dysplasia-cone-rod dystrophy syndrome
Homo sapiens (human)
DOID:0112303
  • spondylometaphyseal dysplasia with corneal dystrophy
  • Aliases:
    • SMDCD
Homo sapiens (human)
DOID:0112313
  • brain small vessel disease
Rattus norvegicus (Norway rat)
DOID:0112313
  • brain small vessel disease
Homo sapiens (human)
DOID:0112313
  • brain small vessel disease
Mus musculus (house mouse)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Danio rerio (zebrafish)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Homo sapiens (human)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Caenorhabditis elegans
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Rattus norvegicus (Norway rat)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Drosophila melanogaster (fruit fly)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Xenopus laevis (African clawed frog)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Mus musculus (house mouse)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Xenopus tropicalis (tropical clawed frog)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Homo sapiens (human)

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Last updated: August 19, 2024