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 3151 - 3175 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:2920
  • membranoproliferative glomerulonephritis
  • Aliases:
    • Lobular glomerulonephritis
    • chronic glomerulonephritis, lobular
Homo sapiens (human)
DOID:10976
  • membranous glomerulonephritis
  • Aliases:
    • membranous nephropathy
Homo sapiens (human)
DOID:8243
  • meningeal melanomatosis
  • Aliases:
    • Leptomeningeal melanomatosis
Homo sapiens (human)
DOID:7614
  • meninges sarcoma
  • Aliases:
    • Meningeal sarcoma
    • sarcoma of meninges
Homo sapiens (human)
DOID:3565
  • meningioma
  • Aliases:
    • meningeal neoplasm
    • meningothelial cell tumor
    • neoplasm of the meninges
    • primary Meningeal tumor
Homo sapiens (human)
DOID:9471
  • meningitis
Homo sapiens (human)
DOID:1088
  • meningocele
Homo sapiens (human)
DOID:0080176
  • meningococcal meningitis
Homo sapiens (human)
DOID:10554
  • meningoencephalitis
Homo sapiens (human)
DOID:7212
  • meningothelial meningioma
  • Aliases:
    • Meningotheliomatous meningioma
Homo sapiens (human)
DOID:4783
  • mesangial proliferative glomerulonephritis
Homo sapiens (human)
DOID:3350
  • mesenchymal cell neoplasm
  • Aliases:
    • benign miscellaneous mesenchymal tumor
    • mesenchymal tumor
Homo sapiens (human)
DOID:13252
  • mesenteric vascular occlusion
Homo sapiens (human)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Homo sapiens (human)
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Homo sapiens (human)
DOID:0111512
  • metachondromatosis
  • Aliases:
    • METCDS
Homo sapiens (human)
DOID:10581
  • metachromatic leukodystrophy
  • Aliases:
    • MLD
    • Scholz cerebral sclerosis
    • arylsulfatase A deficiency
    • deficiency of cerebroside-sulfatase
    • sulfatide lipoidosis
Homo sapiens (human)
DOID:6404
  • metanephric adenoma
Homo sapiens (human)
DOID:10783
  • methemoglobinemia
Homo sapiens (human)
DOID:0060742
  • methylmalonic acidemia cblA type
  • Aliases:
    • methylmalonic aciduria cblA type
    • methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type
Homo sapiens (human)
DOID:0060743
  • methylmalonic acidemia cblB type
  • Aliases:
    • methylmalonic aciduria cblB type
    • methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type
Homo sapiens (human)
DOID:0060741
  • methylmalonic acidemia due to transcobalamin receptor defect
  • Aliases:
    • methylmalonic acidemia, TCblR type
    • methylmalonic aciduria due to transcobalamin receptor defect
Homo sapiens (human)
DOID:14749
  • methylmalonic acidemia
  • Aliases:
    • methylmalonic aciduria
Homo sapiens (human)
DOID:0060740
  • methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
  • Aliases:
    • methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency
    • methylmalonic aciduria mut type
    • vitamin B12-unresponsive methylmalonic aciduria
Homo sapiens (human)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
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