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 4126 - 4150 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:2870
  • endometrial adenocarcinoma
  • Aliases:
    • adenocarcinoma of endometrium
    • adenocarcinoma of the Endometrium
    • adenocarcinoma of uterus
    • endometrial adenoacanthoma
    • endometrial endometrioid adenocarcinoma
    • endometrial endometrioid adenocarcinoma with squamous differentiation
    • endometrioid adenoma or carcinoma
    • endometrioid adenomas and carcinomas
    • endometrioid carcinoma of Endometrium
Mus musculus (house mouse)
DOID:5409
  • lung small cell carcinoma
Mus musculus (house mouse)
DOID:0111454
  • SHORT syndrome
  • Aliases:
    • Aarskog-Ose-Pande syndrome
    • Lipodystrophy-Rieger anomaly-diabetes syndrome
    • Rieger anomaly-partial lipodystrophy syndrome
    • short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay
Mus musculus (house mouse)
DOID:0111949
  • immunodeficiency 36
  • Aliases:
    • IMD36
    • activated phosphoinositide 3-kinase delta syndrome 2
Mus musculus (house mouse)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Mus musculus (house mouse)
DOID:7305
  • astroblastoma
Mus musculus (house mouse)
DOID:0081139
  • agammaglobulinemia 7
Mus musculus (house mouse)
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Caenorhabditis elegans
DOID:0111242
  • congenital muscular dystrophy-dystroglycanopathy type A6
  • Aliases:
    • MDDGA6
    • Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6
Caenorhabditis elegans
DOID:11727
  • facioscapulohumeral muscular dystrophy
  • Aliases:
    • Landouzy Dejerine muscular dystrophy
    • Landouzy-Dejerine muscular dystrophy
    • Muscular dystrophy, Landouzy-Dejerine
Caenorhabditis elegans
DOID:1508
  • candidiasis
  • Aliases:
    • Disseminated candidiasis
    • systemic candidiasis
Caenorhabditis elegans
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Caenorhabditis elegans
DOID:0080411
  • familial adenomatous polyposis 3
Caenorhabditis elegans
DOID:2615
  • papilloma
  • Aliases:
    • papillomatosis
Mus musculus (house mouse)
DOID:883
  • parasitic helminthiasis infectious disease
  • Aliases:
    • helminth infection
    • helminthiasis
    • helminthosis
    • worm infection
Homo sapiens (human)
DOID:4985
  • extraosseous Ewings sarcoma-primitive neuroepithelial tumor
  • Aliases:
    • extraosseous Ewing's tumor
    • extraosseous Ewing's tumour
    • extraosseous Ewings sarcoma-primitive neuroepithelial tumour
Homo sapiens (human)
DOID:4232
  • extraosseous Ewing sarcoma
  • Aliases:
    • extraosseous Ewing's sarcoma
    • extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor
    • extraskeletal Ewing sarcom
Homo sapiens (human)
DOID:0111670
  • primary hyperoxaluria type 1
  • Aliases:
    • HP1
    • alanine-glyoxylate aminotransferase deficiency
    • glycolic aciduria
    • hepatic AGT deficiency
    • oxalosis I
    • peroxisomal alanine-glyoxylate aminotransferase deficiency
    • serine pyruvate aminotransferase deficiency
Homo sapiens (human)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Homo sapiens (human)
DOID:0060074
  • ductal carcinoma in situ
Homo sapiens (human)
DOID:890
  • mitochondrial encephalomyopathy
Homo sapiens (human)
DOID:0080124
  • mitochondrial DNA depletion syndrome 5
  • Aliases:
    • succinate-CoA ligase deficiency
Homo sapiens (human)
DOID:0070331
  • mitochondrial DNA depletion syndrome 8b
  • Aliases:
    • mitochondrial neurogastrointestinal encephalopathy syndrome, RRM2B-related
Homo sapiens (human)
DOID:0080127
  • mitochondrial DNA depletion syndrome 8a
  • Aliases:
    • RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Homo sapiens (human)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Homo sapiens (human)

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Last updated: August 19, 2024