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 1026 - 1050 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Homo sapiens (human)
DOID:3454
  • brain infarction
Homo sapiens (human)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Homo sapiens (human)
DOID:0050847
  • sleep apnea
Homo sapiens (human)
DOID:2722
  • acrodermatitis
Homo sapiens (human)
DOID:10607
  • tropical sprue
  • Aliases:
    • Sprue - tropical
    • Tropical steatorrhea
Homo sapiens (human)
DOID:0080162
  • lupus nephritis
Homo sapiens (human)
DOID:216
  • dental caries
  • Aliases:
    • Dental caries extending into pulp
    • Dental caries of smooth surface
    • Dental caries pit and fissure
Homo sapiens (human)
DOID:10461
  • dentin caries
  • Aliases:
    • Compound dental caries
    • Dental caries extending into dentine
Homo sapiens (human)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Homo sapiens (human)
DOID:6543
  • acne
  • Aliases:
    • Acne varioliformis
    • acne vulgaris
    • frontalis acne
Homo sapiens (human)
DOID:0111415
  • trichohepatoenteric syndrome 1
  • Aliases:
    • THES1
Homo sapiens (human)
DOID:0110227
  • cataract 32 multiple types
  • Aliases:
    • CTRCT32
Homo sapiens (human)
DOID:2752
  • glycogen storage disease II
  • Aliases:
    • Generalized glycogenosis
    • Glycogen storage disease 2
    • Glycogen storage disease, type II
    • Glycogenosis, type 2
    • Lysosomal alpha-1,4-glucosidase deficiency
    • Pompe's disease
    • acid maltase deficiency
    • deficiency of glucoamylase
    • deficiency of maltase
    • glycogen storage disease type II
Homo sapiens (human)
DOID:0111414
  • trichohepatoenteric syndrome
  • Aliases:
    • SD/THE
    • Syndromic diarrhea/Tricho-hepato-enteric syndrome
    • THES
    • Tricho-hepato-enteric syndrome
    • phenotypic diarrhea
    • syndromic diarrhea
Homo sapiens (human)
DOID:14402
  • critical illness polyneuropathy
Homo sapiens (human)
DOID:5679
  • retinal disease
Homo sapiens (human)
DOID:3612
  • retinitis
Homo sapiens (human)
DOID:37
  • skin disease
  • Aliases:
    • Genodermatosis
    • skin and subcutaneous tissue disease
Homo sapiens (human)
DOID:1555
  • urticaria
Homo sapiens (human)
DOID:12712
  • nephronophthisis
  • Aliases:
    • medullary cystic disease
    • medullary cystic kidney
Homo sapiens (human)
DOID:0050576
  • Senior-Loken syndrome
  • Aliases:
    • Loken Senior syndrome
    • renal-retinal syndrome
Homo sapiens (human)
DOID:10300
  • Raynaud disease
  • Aliases:
    • Raynaud's disease
    • Raynaud's syndrome
Homo sapiens (human)
DOID:4562
  • subacute bacterial endocarditis
  • Aliases:
    • Endocarditis lenta
    • SBE - Subacute bacterial endocarditis
    • Subacute endocarditis, lenta
Homo sapiens (human)
DOID:3355
  • fibrosarcoma
  • Aliases:
    • Fibrocytic tumor
    • fibrosarcoma of soft tissue
    • fibrous tissue neoplasm
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