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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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 8201 - 8225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0090067
  • Fuhrmann syndrome
Homo sapiens (human)
DOID:0050788
  • proximal symphalangism
  • Aliases:
    • Cushing's symphalangism
Xenopus laevis (African clawed frog)
DOID:0040085
  • bacterial sepsis
Mus musculus (house mouse)
DOID:0080633
  • developmental cardiac valvular defect
Homo sapiens (human)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Saccharomyces cerevisiae S288C
DOID:3314
  • angiomyolipoma
Drosophila melanogaster (fruit fly)
DOID:1307
  • dementia
Caenorhabditis elegans
DOID:0080416
  • developmental and epileptic encephalopathy 32
  • Aliases:
    • DEE32
    • early infantile epileptic encephalopathy 32
Homo sapiens (human)
DOID:9432
  • renal glycosuria
  • Aliases:
    • renal diabetes
Rattus norvegicus (Norway rat)
DOID:0070249
  • autosomal dominant Emery-Dreifuss muscular dystrophy 4
  • Aliases:
    • EDMD4
    • Emery-Dreifuss muscular dystrophy 4 with variable features
    • Emery-Dreifuss muscular dystrophy 4, autosomal dominant
Homo sapiens (human)
DOID:0110436
  • dilated cardiomyopathy 1L
  • Aliases:
    • CMD1L
Homo sapiens (human)
DOID:0112157
  • X-linked atrophic macular degeneration
Mus musculus (house mouse)
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Drosophila melanogaster (fruit fly)
DOID:3687
  • MELAS syndrome
  • Aliases:
    • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
Mus musculus (house mouse)
DOID:3265
  • chronic granulomatous disease
  • Aliases:
    • Bridges-Good syndrome
    • CGD
    • Congenital dysphagocytosis
    • Quie syndrome
Rattus norvegicus (Norway rat)
DOID:9870
  • galactosemia
  • Aliases:
    • Galactosaemia
    • Galactose intolerance
Saccharomyces cerevisiae S288C
DOID:479
  • angiokeratoma
  • Aliases:
    • Angiokeratoma of skin
    • Cutaneous Angiokeratoma
    • skin angiokeratoma
Mus musculus (house mouse)
DOID:0110247
  • cataract 36
  • Aliases:
    • CATC4
    • CTRCT36
    • autosomal recessive congenital cataract 4
Homo sapiens (human)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Homo sapiens (human)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Mus musculus (house mouse)
DOID:0060010
  • Omenn syndrome
  • Aliases:
    • combined immunodeficiency with hypereosinophilia
Homo sapiens (human)
DOID:9974
  • drug dependence
Danio rerio (zebrafish)
DOID:10983
  • Alport syndrome
  • Aliases:
    • Hereditary Nephritis
Homo sapiens (human)
DOID:0060837
  • isolated microphthalmia 5
  • Aliases:
    • MCOP5
    • microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome
    • posterior microphthalmia with retinitis pigmentosa, foveoschisis and optic disc drusen
Homo sapiens (human)
DOID:1168
  • familial hyperlipidemia
  • Aliases:
    • familial hyperlipoproteinemia
    • hyperlipemia
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: December 9, 2024