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 76 - 100 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:11847
  • coronary thrombosis
  • Aliases:
    • Coronary artery thrombosis
Homo sapiens (human)
DOID:10264
  • mumps
Homo sapiens (human)
DOID:61
  • mitral valve disease
  • Aliases:
    • Mitral RH valve dis.
    • Rheumatic mitral insufficiency
    • Rheumatic mitral valve changes
    • Rheumatic mitral valve regurgitation
    • chronic rheumatic mitral valve
    • disease of mitral valve
    • rheumatic disease of mitral valve
    • rheumatic mitral valve incompetence
Homo sapiens (human)
DOID:47
  • prostate disease
Homo sapiens (human)
DOID:0110259
  • cataract 43
  • Aliases:
    • CTRCT43
Homo sapiens (human)
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Homo sapiens (human)
DOID:6886
  • ureter small cell carcinoma
  • Aliases:
    • ureteral small cell carcinoma
Homo sapiens (human)
DOID:0090101
  • lethal congenital glycogen storage disease of heart
  • Aliases:
    • fatal congenital hypertrophic cardiomyopathy due to GSD
    • fatal congenital hypertrophic cardiomyopathy due to glycogenosis
    • fatal congenital nonlysosomal cardiac glycogenosis
    • phosphorylase kinase deficiency of heart
Homo sapiens (human)
DOID:5304
  • ovarian clear cell adenocarcinoma
Homo sapiens (human)
DOID:0110054
  • amelogenesis imperfecta type 1A
  • Aliases:
    • AI1A
    • amelogenesis imperfecta hypoplastic type IA
    • amelogenesis imperfecta type IA
Homo sapiens (human)
DOID:12241
  • beta thalassemia
Homo sapiens (human)
DOID:5567
  • ovarian germ cell teratoma
  • Aliases:
    • germ cell teratoma of Ovary
Homo sapiens (human)
DOID:12205
  • dengue disease
  • Aliases:
    • Dengue Fever
    • breakbone fever
    • classic dengue
Homo sapiens (human)
DOID:5679
  • retinal disease
Homo sapiens (human)
DOID:0070218
  • familial hyperinsulinemic hypoglycemia 2
  • Aliases:
    • Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
    • HHF2
    • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:4386
  • myofibroma
  • Aliases:
    • Lipoleiomyoma
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)
DOID:5683
  • hereditary breast ovarian cancer syndrome
  • Aliases:
    • BRCA1- and BRCA2-associated hereditary breast and ovarian cancer
    • Breast and Ovarian Cancer syndrome
    • HBOC syndrome
    • Hereditary Breast and Ovarian Cancer syndrome
    • Hereditary breast and ovarian cancer
Homo sapiens (human)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Homo sapiens (human)
DOID:0110845
  • xeroderma pigmentosum group D
  • Aliases:
    • XP group D
    • XP group H
    • XP4
    • XP8
    • XPD
    • XPDC
    • XPH
    • xeroderma pigmentosum IV
    • xeroderma pigmentosum VIII
Homo sapiens (human)
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Homo sapiens (human)
DOID:4889
  • lymph node tuberculosis
  • Aliases:
    • Tuberculous adenitis
    • Tuberculous lymphadenopathy
    • king's evil
    • scrofula
Homo sapiens (human)
DOID:9008
  • psoriatic arthritis
  • Aliases:
    • arthritis psoriatica
    • arthropathic psoriasis
Homo sapiens (human)
DOID:3393
  • coronary artery disease
  • Aliases:
    • CHD
    • Coronary disease
    • coronary arteriosclerosis
    • coronary heart disease
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