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 3126 - 3150 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:8622
  • measles
  • Aliases:
    • morbilli
Homo sapiens (human)
DOID:9306
  • mechanical strabismus
Homo sapiens (human)
DOID:11049
  • meconium aspiration syndrome
  • Aliases:
    • Neonatal aspiration of meconium
    • meconium aspiration
Homo sapiens (human)
DOID:6867
  • mediastinal gray zone lymphoma
Homo sapiens (human)
DOID:6868
  • mediastinal malignant lymphoma
  • Aliases:
    • Lymphoma of mediastinum
Homo sapiens (human)
DOID:819
  • mediastinitis
Homo sapiens (human)
DOID:5292
  • mediastinum leiomyosarcoma
  • Aliases:
    • leiomyosarcoma of mediastinum
Homo sapiens (human)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0050902
  • medulloblastoma
  • Aliases:
    • CNS PNET
    • CPNET
    • Medulloblastoma, histologically defined
    • brain medulloblastoma
    • infratentorial primitive neuroectodermal tumor
    • localized primitive neuroectodermal tumor
Homo sapiens (human)
DOID:4790
  • medulloepithelioma
  • Aliases:
    • Diktyoma, malignant
    • Medulloepithelioma, central nervous system
Homo sapiens (human)
DOID:3861
  • medullomyoblastoma
Homo sapiens (human)
DOID:11372
  • megacolon
  • Aliases:
    • Dilatation of colon
Homo sapiens (human)
DOID:0110632
  • megaconial type congenital muscular dystrophy
  • Aliases:
    • congenital megaconial myopathy
    • congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
    • congenital muscular dystrophy with mitochondrial structural abnormalities
    • megaconial congenital muscular dystrophy
Homo sapiens (human)
DOID:0060610
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • Aliases:
    • Berdon syndrome
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
    • visceral myopathy
Homo sapiens (human)
DOID:13186
  • megaesophagus
Homo sapiens (human)
DOID:13382
  • megaloblastic anemia
  • Aliases:
    • Grasbeck-Imerslund syndrome
    • Imerslund-Grasbeck syndrome
    • MGA1 Norwegian type
    • RH-MGA1
    • megaloblastic anaemia
    • recessive hereditary megaloblastic anaemia 1
    • recessive hereditary megaloblastic anemia 1
Homo sapiens (human)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Homo sapiens (human)
DOID:1595
  • melancholic depression
  • Aliases:
    • endogenous depression
    • major depressive disorder with melancholic features
    • melancholia
Homo sapiens (human)
DOID:11684
  • melanoacanthoma
Homo sapiens (human)
DOID:1909
  • melanoma
  • Aliases:
    • Naevocarcinoma
    • malignant melanoma
Homo sapiens (human)
DOID:3868
  • melanotic medulloblastoma
  • Aliases:
    • Medulloblastoma, melanotic
Homo sapiens (human)
DOID:3205
  • melanotic neurilemmoma
  • Aliases:
    • Melanotic Schwannoma
    • Pigmented Neurilemmoma
    • Pigmented schwannoma
Homo sapiens (human)
DOID:166
  • melanotic neuroectodermal tumor
  • Aliases:
    • Infantile Melanotic neuroectodermal neoplasm
    • Melanotic neuroectodermal tumor of infancy
    • Melanotic neuroectodermal tumour of infancy
    • Pigmented neuroectodermal tumour of infancy
    • melanotic neuroectodermal tumour
Homo sapiens (human)
DOID:5052
  • melioidosis
  • Aliases:
    • Nightcliff gardener's disease
    • Pseudoglanders
    • Whitmore's disease
    • acute and fulminating melioidosis
    • subacute and chronic melioidosis
Homo sapiens (human)
DOID:4253
  • melorheostosis
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024