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 4026 - 4050 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:11914
  • gastroparesis
  • Aliases:
    • Gastroparalysis
    • Gastroparesis syndrome
    • gastric atonia
Homo sapiens (human)
DOID:2224
  • essential thrombocythemia
  • Aliases:
    • Essential thrombocythaemia
    • familial thrombocytosis
    • hemorrhagic thrombocythemia
    • hereditary thrombocythemia
    • primary Thrombocytosis
Drosophila melanogaster (fruit fly)
DOID:8677
  • perinatal necrotizing enterocolitis
  • Aliases:
    • ENTEROCOLITIS NECROTIZING
    • Necrotizing enterocolitis in fetus OR newborn
    • Perinatal necrotising enterocolitis
    • Pseudomembranous enterocolitis in newborn
    • necrotizing enterocolitis
Mus musculus (house mouse)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Homo sapiens (human)
DOID:0050328
  • congenital hypothyroidism
Mus musculus (house mouse)
DOID:9408
  • acute myocardial infarction
Saccharomyces cerevisiae S288C
DOID:9655
  • oral mucosa leukoplakia
Homo sapiens (human)
DOID:12841
  • ancylostomiasis
Homo sapiens (human)
DOID:10964
  • cholesteatoma of middle ear
  • Aliases:
    • Cholesteatoma of middle ear and mastoid
    • Cholesteatoma of middle ear and/or mastoid
    • Cholesteatoma of the middle ear
    • Epidermosis of ear
    • Epidermosis of middle ear
    • middle ear cholesteatoma
Homo sapiens (human)
DOID:8584
  • Burkitt lymphoma
  • Aliases:
    • Burkitt lymphoma/leukaemia
    • Burkitt's Lymphoma
    • Burkitt's tumor
    • Burkitt's tumor or lymphoma
    • malignant lymphoma, Burkitt's type
    • small Non-Cleaved cell Lymphoma, Burkitt's type
Drosophila melanogaster (fruit fly)
DOID:0110763
  • hereditary spastic paraplegia 10
  • Aliases:
    • SPG10
    • autosomal dominant spastic paraplegia 10
    • autosomal dominant spastic paraplegia type 10
Homo sapiens (human)
DOID:12978
  • Plasmodium vivax malaria
  • Aliases:
    • Malaria by Plasmodium vivax
    • Vivax Malaria
Homo sapiens (human)
DOID:0110443
  • dilated cardiomyopathy 1B
Xenopus laevis (African clawed frog)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Saccharomyces cerevisiae S288C
DOID:14115
  • toxic shock syndrome
  • Aliases:
    • TSS
    • toxic shock
Caenorhabditis elegans
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Danio rerio (zebrafish)
DOID:1993
  • rectum cancer
  • Aliases:
    • carcinoma of rectum
    • carcinoma of the rectum
    • malignant Rectal tumor
    • malignant neoplasm of rectum
    • malignant rectum tumor
    • malignant tumor of rectum
    • rectal cancer
Homo sapiens (human)
DOID:9975
  • cocaine dependence
Rattus norvegicus (Norway rat)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Caenorhabditis elegans
DOID:4193
  • intracranial thrombosis
  • Aliases:
    • cerebral thrombosis
Homo sapiens (human)
DOID:0110960
  • Gaucher's disease perinatal lethal
  • Aliases:
    • Fetal Gaucher Disease
    • Gaucher Disease, Collodion Type
Mus musculus (house mouse)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Drosophila melanogaster (fruit fly)
DOID:0060316
  • orofaciodigital syndrome I
  • Aliases:
    • Papillon-Leage-Psaume syndrome
    • orofaciodigital syndrome 1
    • orofaciodigital syndrome type I
Homo sapiens (human)
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Mus musculus (house mouse)
DOID:0110306
  • autosomal dominant limb-girdle muscular dystrophy type 3
  • Aliases:
    • LGMD1G
    • autosomal dominant limb-girdle muscular dystrophy type 1G
    • muscular dystrophy limb-girdle type 1G
Homo sapiens (human)

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