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 3101 - 3125 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:8503
  • impetigo herpetiformis
Homo sapiens (human)
DOID:10488
  • imperforate anus
  • Aliases:
    • Congenital atresia of anus
    • Congenital or infantile occlusion of anus
    • anal atresia
Homo sapiens (human)
DOID:0060025
  • immunoglobulin alpha deficiency
  • Aliases:
    • IgA deficiency
    • gamma-A-globulin deficiency
Homo sapiens (human)
DOID:0060758
  • immunodeficiency with hyper-IgM type 2
  • Aliases:
    • AID deficiency
    • HIGM2
    • activation-induced cytidine deaminase deficiency
    • hyper-IgM syndrome type 2
Homo sapiens (human)
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: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
Homo sapiens (human)
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
Saccharomyces cerevisiae S288C
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
Caenorhabditis elegans
DOID:0060023
  • immunodeficiency with hyper IgM type 3
  • Aliases:
    • CD40 deficiency
    • HIGM3
    • hyper-IgM syndrome due to CD40 deficiency
    • type 3 hyper-IgM immunodeficiency
Homo sapiens (human)
DOID:0112002
  • immunodeficiency 47
  • Aliases:
    • CDG IIs
    • CDG2S
    • CDGIIs
    • IMD47
    • congenital disorder of glycosylation type IIs
    • immunodeficiency and hepatopathy with or without neurologic features
Homo sapiens (human)
DOID:0111949
  • immunodeficiency 36
  • Aliases:
    • IMD36
    • activated phosphoinositide 3-kinase delta syndrome 2
Mus musculus (house mouse)
DOID:0111949
  • immunodeficiency 36
  • Aliases:
    • IMD36
    • activated phosphoinositide 3-kinase delta syndrome 2
Rattus norvegicus (Norway rat)
DOID:0111953
  • immunodeficiency 23
  • Aliases:
    • CID due to PGM3 deficiency
    • IMD23
    • PGM3-CDG
    • PGM3-related congenital disorder of glycosylation
    • combined immunodeficiency due to PGM3 deficiency
Homo sapiens (human)
DOID:0111953
  • immunodeficiency 23
  • Aliases:
    • CID due to PGM3 deficiency
    • IMD23
    • PGM3-CDG
    • PGM3-related congenital disorder of glycosylation
    • combined immunodeficiency due to PGM3 deficiency
Saccharomyces cerevisiae S288C
DOID:0111953
  • immunodeficiency 23
  • Aliases:
    • CID due to PGM3 deficiency
    • IMD23
    • PGM3-CDG
    • PGM3-related congenital disorder of glycosylation
    • combined immunodeficiency due to PGM3 deficiency
Mus musculus (house mouse)
DOID:0111936
  • immunodeficiency 14
  • Aliases:
    • APDS
    • IMD14
    • PASLI disease
    • activated PI3K-delta syndrome
    • senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
Homo sapiens (human)
DOID:4784
  • immune-complex glomerulonephritis
  • Aliases:
    • Immune Complex Glomerulonephritis
Homo sapiens (human)
DOID:2914
  • immune system disease
Homo sapiens (human)
DOID:0090110
  • immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
  • Aliases:
    • Autoimmune enteropathy type 1
    • DMSD
    • IDDM-secretory diarrhea syndrome
    • IPEX
    • X-linked autoimmunity-allergic dysregulation syndrome
    • XLAAD
    • XPID
    • autoimmunity-immunodeficiency syndrome, X-linked
    • diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
    • diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
    • immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
    • immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked
Homo sapiens (human)
DOID:8440
  • ileus
  • Aliases:
    • Ileus of intestine
Homo sapiens (human)
DOID:0060190
  • ileocolitis
Homo sapiens (human)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Drosophila melanogaster (fruit fly)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Rattus norvegicus (Norway rat)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Homo sapiens (human)
DOID:0060189
  • ileitis
  • Aliases:
    • Crohn's ileitis
Mus musculus (house mouse)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024