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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 3126 - 3150 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:218
  • ascending colon cancer
  • Aliases:
    • Ca ascending colon
    • malignant neoplasm of right colon
    • malignant tumor of ascending colon
Xenopus tropicalis (tropical clawed frog)
DOID:0110959
  • Gaucher's disease type III
  • Aliases:
    • GD III
    • Gaucher Disease, Chronic Neuronopathic Type
    • Gaucher Disease, Juvenile And Adult, Cerebral
    • Gaucher Disease, Subacute Neuronopathic Type
Homo sapiens (human)
DOID:0112091
  • nuclear type mitochondrial complex I deficiency 34
  • Aliases:
    • MC1DN34
Homo sapiens (human)
DOID:0080612
  • anterior segment dysgenesis 7
Caenorhabditis elegans
DOID:0081144
  • common variable immunodeficiency 1
Homo sapiens (human)
DOID:1849
  • cannabis dependence
Caenorhabditis elegans
DOID:0111729
  • familial episodic pain syndrome 1
  • Aliases:
    • FEPS1
Mus musculus (house mouse)
DOID:0110527
  • autosomal recessive nonsyndromic deafness 8
  • Aliases:
    • DFNB10
    • DFNB8
    • NRSD8
    • autosomal recessive deafness 10
    • autosomal recessive deafness 8
    • childhood-onset neurosensory autosomal recessive deafness 8
    • neurosensory nonsyndromic recessive deafness 8
Homo sapiens (human)
DOID:13258
  • typhoid fever
  • Aliases:
    • Typhoid
Danio rerio (zebrafish)
DOID:0111337
  • Jackson-Weiss syndrome
  • Aliases:
    • JWS
    • craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome
Mus musculus (house mouse)
DOID:4079
  • heart valve disease
  • Aliases:
    • Valvular heart disease
Drosophila melanogaster (fruit fly)
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
Rattus norvegicus (Norway rat)
DOID:0110146
  • Bartter disease type 4b
  • Aliases:
    • BARTS4B
    • Bartter syndrome, type 4b, digenic
    • neonatal Bartter syndrome type 4B with sensorineural deafness
Mus musculus (house mouse)
DOID:1496
  • echinococcosis
  • Aliases:
    • Echinococcosis of liver
    • echinococcal disease
    • hepatic echinococcosis
    • hydatid disease
    • hydatidosis
    • liver echinococcus
    • pulmonary echinococcosis
Rattus norvegicus (Norway rat)
DOID:2256
  • osteochondrodysplasia
  • Aliases:
    • Cartilage Development disorder
    • Congenital anomaly of cartilage
    • Osteochondrodysplasia syndrome
    • chondrodystrophy
    • skeletal dysplasia
Drosophila melanogaster (fruit fly)
DOID:0080923
  • bilateral parasagittal parieto-occipital polymicrogyria
  • Aliases:
    • bilateral temporooccipital polymicrogyria
Saccharomyces cerevisiae S288C
DOID:399
  • tuberculosis
Mus musculus (house mouse)
DOID:0111102
  • maturity-onset diabetes of the young type 3
  • Aliases:
    • MODY type 3
    • MODY3
Homo sapiens (human)
DOID:0111726
  • geleophysic dysplasia 2
  • Aliases:
    • GPHYSD2
Caenorhabditis elegans
DOID:11512
  • Budd-Chiari syndrome
  • Aliases:
    • hepatic vein thrombosis
Mus musculus (house mouse)
DOID:4992
  • optic nerve glioma
  • Aliases:
    • glioma of the optic nerve
Mus musculus (house mouse)
DOID:0090129
  • carnitine palmitoyltransferase I deficiency
  • Aliases:
    • CPT I deficiency
    • CPT1A deficiency
    • L-CPT1 deficiency
    • carnitine palmitoyl transferase 1A deficiency
    • carnitine palmitoyl transferase IA deficiency
    • hepatic CPT deficiency type I
    • hepatic carnitine palmitoyl transferase 1 deficiency
    • hepatic carnitine palmitoyl transferase I deficiency
Rattus norvegicus (Norway rat)
DOID:0050649
  • atransferrinemia
  • Aliases:
    • familial hypotransferrinemia
Mus musculus (house mouse)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Caenorhabditis elegans
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Mus musculus (house mouse)
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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024