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 1826 - 1850 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:206
  • hereditary multiple exostoses
  • Aliases:
    • Multiple congenital exostosis
    • Multiple exostosis syndromes
    • Osteochondromatosis syndrome
    • hereditary multiple exostoses 1
    • hereditary multiple exostoses 2
    • hereditary multiple exostoses 3
    • multiple ostechondromas
Drosophila melanogaster (fruit fly)
DOID:0111063
  • hyperphosphatemic familial tumoral calcinosis
  • Aliases:
    • HFTC
    • HHS
    • PHPTC
    • cortical hyperostosis with hyperphosphatemia
    • familial Teutschlaender disease
    • familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
    • hypercalcemic tumoral calcinosis
    • hyperostosis with hyperphosphatemia
    • hyperphosphatemia hyperostosis
    • hyperphosphatemia hyperostosis syndrome
    • hyperphosphatemia tumoral calcinosis
    • lipocalcinogranulomatosis
    • morbus Teutschlaender
    • primary hyperphosphatemic tumoral calcinosis
    • tumoral calcinosis with hyperphosphatemia
Rattus norvegicus (Norway rat)
DOID:28
  • endocrine system disease
Drosophila melanogaster (fruit fly)
DOID:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Drosophila melanogaster (fruit fly)
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Drosophila melanogaster (fruit fly)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Drosophila melanogaster (fruit fly)
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Drosophila melanogaster (fruit fly)
DOID:0050877
  • pancreatic agenesis
  • Aliases:
    • Agenesis of the dorsal pancreas
    • partial pancreatic agenesis
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Rattus norvegicus (Norway rat)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:9857
  • interstitial keratitis
Homo sapiens (human)
DOID:0060713
  • autosomal recessive congenital ichthyosis 4B
  • Aliases:
    • ARCI4B
    • harlequin ichthyosis
    • harlequin type ichthyosis congenita
    • harlequin type ichthyosis fetalis
Rattus norvegicus (Norway rat)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Rattus norvegicus (Norway rat)
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
Rattus norvegicus (Norway rat)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Rattus norvegicus (Norway rat)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Rattus norvegicus (Norway rat)
DOID:0070014
  • autosomal dominant dyskeratosis congenita 1
  • Aliases:
    • DKCA1
    • Dyskeratosis Congenita, Scoggins Type
Homo sapiens (human)
DOID:0111108
  • maturity-onset diabetes of the young type 10
  • Aliases:
    • MODY10
Homo sapiens (human)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Rattus norvegicus (Norway rat)
DOID:0110292
  • autosomal recessive limb-girdle muscular dystrophy type 2O
  • Aliases:
    • LGMD2O
    • MDDGC3
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
    • muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
Rattus norvegicus (Norway rat)
DOID:0111236
  • congenital muscular dystrophy-dystroglycanopathy type A3
  • Aliases:
    • MDDGA3
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3
Rattus norvegicus (Norway rat)
DOID:0112378
  • muscular dystrophy-dystroglycanopathy type B3
  • Aliases:
    • MDDGB3
    • congenital muscular dystrophy POMGNT1-related
Rattus norvegicus (Norway rat)
DOID:0050453
  • lissencephaly
Rattus norvegicus (Norway rat)
DOID:0080555
  • congenital disorder of glycosylation Ic
  • Aliases:
    • congenital disorder of glycosylation 1c
Rattus norvegicus (Norway rat)

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Last updated: August 19, 2024