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 3426 - 3450 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Homo sapiens (human)
DOID:119
  • vaginal cancer
  • Aliases:
    • malignant neoplasm of vagina
    • malignant tumor of vagina
    • malignant vaginal tumor
    • neoplasm of vagina
    • vagina neoplasm
    • vaginal tumor
Homo sapiens (human)
DOID:5289
  • uterus leiomyosarcoma
  • Aliases:
    • leiomyosarcoma of Corpus Uteri
Homo sapiens (human)
DOID:4310
  • smooth muscle tumor
Homo sapiens (human)
DOID:5241
  • hemangioblastoma
  • Aliases:
    • Capillary Hemangioblastoma
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Homo sapiens (human)
DOID:3213
  • demyelinating disease
  • Aliases:
    • demyelinating disorder
Homo sapiens (human)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Mus musculus (house mouse)
DOID:11724
  • limb-girdle muscular dystrophy
  • Aliases:
    • Erb's muscular dystrophy
    • Leyden-Mbius muscular dystrophy
    • limb girdle muscular dystrophy
Mus musculus (house mouse)
DOID:720
  • normocytic anemia
  • Aliases:
    • ANEMIA NORMOCYTIC
Homo sapiens (human)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Mus musculus (house mouse)
DOID:7532
  • squamous papillomatosis
Homo sapiens (human)
DOID:0060640
  • ethylmalonic encephalopathy
Homo sapiens (human)
DOID:0080559
  • congenital disorder of glycosylation Ig
  • Aliases:
    • ALG12-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1g
Mus musculus (house mouse)
DOID:0060759
  • immunodeficiency with hyper IgM type 5
  • Aliases:
    • HIGM5
    • hyper-IgM syndrome 5
    • hyper-IgM syndrome due to UNG deficiency
    • hyper-IgM syndrome due to uracil N-glycosylase
Mus musculus (house mouse)
DOID:11702
  • dysgammaglobulinemia
Mus musculus (house mouse)
DOID:0050833
  • orotic aciduria
Mus musculus (house mouse)
DOID:3805
  • porokeratosis
  • Aliases:
    • disseminated superficial actinic porokeratosis
Homo sapiens (human)
DOID:100
  • intestinal infectious disease
  • Aliases:
    • bacterial enteritis
Homo sapiens (human)
DOID:5062
  • phencyclidine abuse
  • Aliases:
    • PCP abuse
Homo sapiens (human)
DOID:5691
  • visual cortex disease
  • Aliases:
    • visual cortex dysfunction
Homo sapiens (human)
DOID:0050145
  • adenoiditis
  • Aliases:
    • chronic adenoiditis
Homo sapiens (human)
DOID:5078
  • ganglioglioma
  • Aliases:
    • CNS ganglioglioma
    • adult ganglioglioma
    • childhood ganglioglioma
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)
DOID:1455
  • geographic tongue
  • Aliases:
    • Glossitis areata exfoliativa
    • Pityriasis linguae
    • benign migratory glossitis
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