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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4501 - 4525 of 5716 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:2723
  • dermatitis
  • Aliases:
    • eczema
    • skin inflammation
Homo sapiens (human)
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Homo sapiens (human)
DOID:11396
  • pulmonary edema
Homo sapiens (human)
DOID:3021
  • acute kidney failure
Homo sapiens (human)
DOID:14115
  • toxic shock syndrome
  • Aliases:
    • TSS
    • toxic shock
Homo sapiens (human)
DOID:9452
  • steatotic liver disease
  • Aliases:
    • Fatty change of liver
    • SLD
    • Steatosis of liver
    • alcoholic fatty liver
    • fatty liver disease
    • hepatic lipidosis
    • hepatic steatosis
Homo sapiens (human)
DOID:0070599
  • X-linked spermatogenic failure 8
  • Aliases:
    • SPGFX8
Homo sapiens (human)
DOID:12798
  • mucopolysaccharidosis
Homo sapiens (human)
DOID:0081168
  • HMG-CoA synthase 2 deficiency
  • Aliases:
    • 3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency
Mus musculus (house mouse)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Homo sapiens (human)
DOID:0112000
  • immunodeficiency 34
  • Aliases:
    • AMCBX2
    • IMD34
    • X-linked MSMD due to CYBB deficiency
    • X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
    • familial atypical mycobacteriosis X-linked 2
    • immunodeficiency 34, mycobacteriosis, X-linked
Homo sapiens (human)
DOID:3265
  • chronic granulomatous disease
  • Aliases:
    • Bridges-Good syndrome
    • CGD
    • Congenital dysphagocytosis
    • Quie syndrome
Homo sapiens (human)
DOID:11664
  • nephrosclerosis
  • Aliases:
    • renal sclerosis
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Homo sapiens (human)
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Homo sapiens (human)
DOID:1059
  • intellectual disability
Mus musculus (house mouse)
DOID:0110497
  • autosomal recessive nonsyndromic deafness 39
  • Aliases:
    • DFNB39
    • autosomal recessive deafness 39
Mus musculus (house mouse)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Mus musculus (house mouse)
DOID:0110569
  • autosomal dominant nonsyndromic deafness 44
  • Aliases:
    • DFNA44
    • autosomal dominant deafness 44
Homo sapiens (human)
DOID:0050746
  • mantle cell lymphoma
Homo sapiens (human)
DOID:3323
  • Sandhoff disease
  • Aliases:
    • Sandhoff Jatzkewitz disease
Mus musculus (house mouse)
DOID:3320
  • Tay-Sachs disease
  • Aliases:
    • GM2 gangliosidosis, type 1
    • hexosaminidase A deficiency
Mus musculus (house mouse)
DOID:870
  • neuropathy
  • Aliases:
    • peripheral neuropathy
Homo sapiens (human)
DOID:6000
  • congestive heart failure
  • Aliases:
    • CHF
    • Cardiac Failure Congestive
    • Congestive heart disease
    • Weak heart
Homo sapiens (human)
DOID:13884
  • sick sinus syndrome
  • Aliases:
    • sinus node infection
Mus musculus (house mouse)
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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: April 7, 2025