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 1426 - 1450 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:8729
  • milker's nodule
  • Aliases:
    • Milkers' node
    • Paravaccinia
    • milker nodule
Homo sapiens (human)
DOID:4376
  • milk allergy
  • Aliases:
    • milk allergic reaction
Homo sapiens (human)
DOID:9861
  • miliary tuberculosis
  • Aliases:
    • Disseminated tuberculosis
    • Tuberculosis miliaris disseminata
    • acute miliary tuberculosis
    • generalized tuberculosis
Homo sapiens (human)
DOID:10590
  • mild pre-eclampsia
Homo sapiens (human)
DOID:6364
  • migraine
  • Aliases:
    • migraine disorder
    • migraine variant
    • migraine with or without aura
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Homo sapiens (human)
DOID:3525
  • middle cerebral artery infarction
Homo sapiens (human)
DOID:0060775
  • microvillus inclusion disease
  • Aliases:
    • Davidson disease
    • MVD
    • congenital familial protracted diarrhea with enterocyte brush-border abnormalities
    • congenital microvillus atrophy
    • diarrhea 2 with microvillus atrophy
    • intractable diarrhea of infancy
Homo sapiens (human)
DOID:4271
  • microsporidiosis
  • Aliases:
    • Infection by Microspora
    • Infection by Microsporea
    • Infection by Microsporida
Homo sapiens (human)
DOID:0060182
  • microscopic colitis
Homo sapiens (human)
DOID:10629
  • microphthalmia
  • Aliases:
    • microphthalmos
    • simple microphthalmos
Homo sapiens (human)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Homo sapiens (human)
DOID:10541
  • microinvasive gastric cancer
  • Aliases:
    • Surface gastric cancer
    • early gastric cancer
Homo sapiens (human)
DOID:5998
  • microglandular adenosis
  • Aliases:
    • Adenosis - breast
    • Adenosis of the breast
Homo sapiens (human)
DOID:11252
  • microcytic anemia
Homo sapiens (human)
DOID:4594
  • microcystic meningioma
Homo sapiens (human)
DOID:5403
  • microcystic adenoma
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Homo sapiens (human)
DOID:0060609
  • microcephalic osteodysplastic primordial dwarfism type II
  • Aliases:
    • Majewski osteodysplastic primordial dwarfism type II
    • osteodysplastic primordial dwarfism type II
Homo sapiens (human)
DOID:0060608
  • microcephalic osteodysplastic primordial dwarfism type I
  • Aliases:
    • Taybi-Linder syndrome
    • brachymelic primordial dwarfism
    • cephaloskeletal dysplasia
    • low-birth-weight dwarfism with skeletal dysplasia
    • osteodysplastic primordial dwarfism type I
Homo sapiens (human)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
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:14749
  • methylmalonic acidemia
  • Aliases:
    • methylmalonic aciduria
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)

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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