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 3326 - 3350 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:5166
  • endometrial stromal tumor
  • Aliases:
    • endometrial Stromal neoplasm
Homo sapiens (human)
DOID:11968
  • postmenopausal atrophic vaginitis
  • Aliases:
    • Senile vaginitis
    • atrophic vaginitis
Homo sapiens (human)
DOID:0080011
  • bone resorption disease
Homo sapiens (human)
DOID:3603
  • mucinous cystadenocarcinoma
  • Aliases:
    • Pseudomucinous cystadenocarcinoma
Homo sapiens (human)
DOID:12554
  • hemolytic-uremic syndrome
  • Aliases:
    • haemolytic-uraemic syndrome
    • hemolytic uremic syndrome
Homo sapiens (human)
DOID:9182
  • pemphigus
Homo sapiens (human)
DOID:0060851
  • pemphigus vulgaris
  • Aliases:
    • familial pemphigus vulgaris
Homo sapiens (human)
DOID:11701
  • selective IgA deficiency disease
  • Aliases:
    • Immunoglobulin A deficiency
    • Selective immunoglobulin A deficiency
    • selective IgA immunodeficiency
Homo sapiens (human)
DOID:0060025
  • immunoglobulin alpha deficiency
  • Aliases:
    • IgA deficiency
    • gamma-A-globulin deficiency
Homo sapiens (human)
DOID:9663
  • aphthous stomatitis
  • Aliases:
    • Aphtha
    • Aphthous ulceration
    • Canker sore
    • Oral aphthae
    • oral ulcer
Homo sapiens (human)
DOID:9271
  • ornithine carbamoyltransferase deficiency
  • Aliases:
    • deficiency of citrulline phosphorylase
    • ornithine transcarbamylase deficiency
Homo sapiens (human)
DOID:0111416
  • trichohepatoenteric syndrome 2
  • Aliases:
    • THES2
Homo sapiens (human)
DOID:14757
  • Ehlers-Danlos syndrome hypermobility type
  • Aliases:
    • Ehlers-Danlos syndrome, type 3
    • type III Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:0050445
  • X-linked dominant hypophosphatemic rickets
  • Aliases:
    • Hypophosphatemia, Vitamin D-Resistant Rickets
    • Vitamin D-Resistant Rickets, X-Linked
    • X-linked hypophosphatemia
    • hypophosphatemic rickets X-linked dominant
Homo sapiens (human)
DOID:1752
  • ocular melanoma
  • Aliases:
    • eye melanoma
    • intraocular melanoma
    • melanoma of eye
Homo sapiens (human)
DOID:10983
  • Alport syndrome
  • Aliases:
    • Hereditary Nephritis
Homo sapiens (human)
DOID:2347
  • generalized atherosclerosis
  • Aliases:
    • Generalised atherosclerosis
Homo sapiens (human)
DOID:0060700
  • familial hypocalciuric hypercalcemia 1
  • Aliases:
    • FHH type 1
    • HHC1
    • familial benign hypercalcemia 1
    • familial hypocalciuric hypercalcemia type I
    • hypocalciuric hypercalcemia type I
Homo sapiens (human)
DOID:3149
  • keratoacanthoma
Homo sapiens (human)
DOID:0050860
  • colorectal adenoma
Homo sapiens (human)
DOID:6945
  • inverted follicular keratosis
  • Aliases:
    • Inverted folicular keratosis
Homo sapiens (human)
DOID:11684
  • melanoacanthoma
Homo sapiens (human)
DOID:13197
  • nodular goiter
  • Aliases:
    • Goiter, nodular
    • nodular goitre
Homo sapiens (human)
DOID:1602
  • lymphadenitis
  • Aliases:
    • Adenitis
    • Inflammation of lymph node
    • acute adenitis
    • acute lymphadenitis
    • chronic Lymphadenitis
    • chronic adenitis
Homo sapiens (human)
DOID:355
  • mast-cell sarcoma
Homo sapiens (human)

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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