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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 2226 - 2250 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:4929
  • tubular adenocarcinoma
  • Aliases:
    • tubular carcinoma
Homo sapiens (human)
DOID:5031
  • adult pineal parenchymal tumor
  • Aliases:
    • adult Pineal Parenchymal neoplasm
Homo sapiens (human)
DOID:0112063
  • X-Linked immunodeficiency 74
  • Aliases:
    • IMD74
    • TLR7 deficiency
    • X-linked immunodeficiency 74,COVID-19-related
    • respiratory insufficiency due to SARS-CoV-2 viral infection
Homo sapiens (human)
DOID:0111578
  • Gillespie syndrome
  • Aliases:
    • GLSP
    • aniridia, cerebellar ataxia and mental deficiency
    • aniridia-cerebellar ataxia-intellectual disability syndrome
Homo sapiens (human)
DOID:0111131
  • focal segmental glomerulosclerosis 6
  • Aliases:
    • FSGS6
Homo sapiens (human)
DOID:0080566
  • congenital disorder of glycosylation In
  • Aliases:
    • congenital disorder of glycosylation 1n
Homo sapiens (human)
DOID:0060597
  • atypical chronic myeloid leukemia, BCR-ABL1 negative
  • Aliases:
    • aCML
    • atypical CML
    • atypical chronic myeloid leukaemia
    • atypical chronic myeloid leukaemia BCR-ABL1 negative
    • atypical chronic myeloid leukemia BCR-ABL1 negative
    • subacute myeloid leukemia
Homo sapiens (human)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Homo sapiens (human)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Homo sapiens (human)
DOID:0070411
  • autosomal recessive spinocerebellar ataxia 30
  • Aliases:
    • SCAR30
Homo sapiens (human)
DOID:10459
  • common cold
  • Aliases:
    • Acute viral rhinopharyngitis
    • Nasopharyngitis - acute
    • Nasopharyngitis, acute
    • acute coryza
    • acute nasopharyngitis
    • acute rhinitis
    • rhino-sinusitis
Homo sapiens (human)
DOID:10937
  • impulse control disorder
Homo sapiens (human)
DOID:0060577
  • 3MC syndrome 3
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:10300
  • Raynaud disease
  • Aliases:
    • Raynaud's disease
    • Raynaud's syndrome
Homo sapiens (human)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Homo sapiens (human)
DOID:0110297
  • autosomal recessive limb-girdle muscular dystrophy type 2K
  • Aliases:
    • LGMD2K
    • MDDGC1
    • limb-girdle muscular dystrophy-intellectual disability syndrome
    • muscular dystrophy limb-girdle type 2K
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1
Homo sapiens (human)
DOID:12799
  • mucopolysaccharidosis II
  • Aliases:
    • Hunter syndrome
    • Hunter's syndrome
    • MPS II - Hunter syndrome
    • Mucopolysaccharidosis, MPS-II
    • deficiency of iduronate-2-sulphatase
Homo sapiens (human)
DOID:10534
  • stomach cancer
  • Aliases:
    • gastric cancer
    • gastric neoplasm
Homo sapiens (human)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Homo sapiens (human)
DOID:0080465
  • developmental and epileptic encephalopathy 30
  • Aliases:
    • DEE30
    • early infantile epileptic encephalopathy 30
Homo sapiens (human)
DOID:11569
  • neurocirculatory asthenia
  • Aliases:
    • Cardiovascular malfunction arising from mental factors
    • Cardiovascular neurosis
    • Da Costa's syndrome
    • Krishaber's disease
Homo sapiens (human)
DOID:0050602
  • triple-A syndrome
  • Aliases:
    • AAAS
    • Achalasia-Addisonianism-Alacrimia syndrome
    • Allgrove Syndrome
Homo sapiens (human)
DOID:0112341
  • hereditary spastic paraplegia 80
  • Aliases:
    • SPG80
    • spastic paraplegia 80 autosomal dominant
Homo sapiens (human)
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Last updated: February 17, 2025