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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 8526 - 8550 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111369
  • hyperalphalipoproteinemia 1
  • Aliases:
    • HALP1
Homo sapiens (human)
DOID:0111366
  • familial hepatic adenoma
  • Aliases:
    • familial liver cell adenomas
Homo sapiens (human)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Homo sapiens (human)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Drosophila melanogaster (fruit fly)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Mus musculus (house mouse)
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Mus musculus (house mouse)
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Caenorhabditis elegans
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Homo sapiens (human)
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Rattus norvegicus (Norway rat)
DOID:0111363
  • Heinz body anemia
Mus musculus (house mouse)
DOID:0111363
  • Heinz body anemia
Saccharomyces cerevisiae S288C
DOID:0111363
  • Heinz body anemia
Homo sapiens (human)
DOID:0111359
  • large congenital melanocytic nevus
  • Aliases:
    • Congenital pigmented nevus
    • GMN
    • Giant congenital melanocytic nevus
    • Giant pigmented hairy nevus
    • LCMN
Homo sapiens (human)
DOID:0111358
  • Floating-Harbor syndrome
  • Aliases:
    • FLHS
Homo sapiens (human)
DOID:0111354
  • arthrogryposis, renal dysfunction, and cholestasis 2
  • Aliases:
    • ARCS2
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Rattus norvegicus (Norway rat)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Mus musculus (house mouse)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Homo sapiens (human)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Saccharomyces cerevisiae S288C
DOID:0111351
  • D-2-hydroxyglutaric aciduria 1
  • Aliases:
    • D2HGA1
Homo sapiens (human)
DOID:0111349
  • hereditary desmoid disease
  • Aliases:
    • FIF
    • familial infiltrative fibromatosis
Homo sapiens (human)
DOID:0111348
  • multiple epiphyseal dysplasia with myopia and deafness
  • Aliases:
    • EDMMD
    • multiple epiphyseal dysplasia, Beighton type
    • multiple epiphyseal dysplasia-myopia-deafness syndrome
Xenopus laevis (African clawed frog)
DOID:0111348
  • multiple epiphyseal dysplasia with myopia and deafness
  • Aliases:
    • EDMMD
    • multiple epiphyseal dysplasia, Beighton type
    • multiple epiphyseal dysplasia-myopia-deafness syndrome
Mus musculus (house mouse)
DOID:0111348
  • multiple epiphyseal dysplasia with myopia and deafness
  • Aliases:
    • EDMMD
    • multiple epiphyseal dysplasia, Beighton type
    • multiple epiphyseal dysplasia-myopia-deafness syndrome
Homo sapiens (human)
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024