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 2076 - 2100 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:3772
  • intraventricular meningioma
Homo sapiens (human)
DOID:7212
  • meningothelial meningioma
  • Aliases:
    • Meningotheliomatous meningioma
Homo sapiens (human)
DOID:7210
  • psammomatous meningioma
Homo sapiens (human)
DOID:6869
  • parasagittal meningioma
Homo sapiens (human)
DOID:6548
  • angiomatous meningioma
Homo sapiens (human)
DOID:4594
  • microcystic meningioma
Homo sapiens (human)
DOID:4210
  • clear cell meningioma
Homo sapiens (human)
DOID:7213
  • transitional meningioma
  • Aliases:
    • transitional (mixed) meningioma
Homo sapiens (human)
DOID:4587
  • benign meningioma
  • Aliases:
    • meningioma, benign
Homo sapiens (human)
DOID:7211
  • fibrous meningioma
  • Aliases:
    • Fibroblastic meningioma
Homo sapiens (human)
DOID:6114
  • cerebral convexity meningioma
  • Aliases:
    • Cerebral Hemispheric Convexity meningioma
Homo sapiens (human)
DOID:8057
  • olfactory groove meningioma
  • Aliases:
    • meningioma of the Olfactory Groove
Homo sapiens (human)
DOID:4141
  • intraorbital meningioma
Homo sapiens (human)
DOID:1138
  • spinal meningioma
  • Aliases:
    • Spinal Cord meningioma
Homo sapiens (human)
DOID:4591
  • lymphoplasmacyte-rich meningioma
  • Aliases:
    • Lymphoplasmocyte-rich meningioma
Homo sapiens (human)
DOID:0111531
  • bilateral optic nerve hypoplasia
  • Aliases:
    • ONH
    • familial bilateral optic nerve hypoplasia
    • isolated optic nerve hypoplasia/aplasia
Homo sapiens (human)
DOID:9574
  • choanal atresia
  • Aliases:
    • Atresia of nares
    • Imperforate nares
    • posterior choanal atresia
Homo sapiens (human)
DOID:0050638
  • transthyretin amyloidosis
  • Aliases:
    • ATTR amyloidosis
    • ATTRm amyloidosis
    • Amyloidosis, hereditary, transthyretin-related
    • Corino de Andrade's disease
    • Familial transthyretin amyloidosis
    • TTR amyloidosis
    • familial amyloid polyneuropathy
    • paramyloidosis
    • transthyretin-related hereditary amyloidosis
Homo sapiens (human)
DOID:0060840
  • isolated microphthalmia 1
  • Aliases:
    • MCOP1
Homo sapiens (human)
DOID:0060842
  • isolated microphthalmia 3
  • Aliases:
    • MCOP3
Homo sapiens (human)
DOID:0060839
  • isolated microphthalmia 2
  • Aliases:
    • MCOP2
Homo sapiens (human)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Homo sapiens (human)
DOID:0060838
  • isolated microphthalmia 7
  • Aliases:
    • MCOP7
Homo sapiens (human)
DOID:0060841
  • isolated microphthalmia 8
  • Aliases:
    • MCOP8
Homo sapiens (human)
DOID:0060836
  • isolated microphthalmia 4
  • Aliases:
    • MCOP4
Homo sapiens (human)

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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: August 19, 2024