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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 6076 - 6100 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Rattus norvegicus (Norway rat)
DOID:1192
  • peripheral nervous system neoplasm
  • Aliases:
    • neoplasm of peripheral nerve
    • nerve sheath neoplasm
    • tumor of PNS
Homo sapiens (human)
DOID:11695
  • portal vein thrombosis
Xenopus laevis (African clawed frog)
DOID:1749
  • squamous cell carcinoma
  • Aliases:
    • epidermoid carcinoma
    • malignant squamous cell tumor
    • squamous carcinoma
    • squamous cell Epithelioma
    • squamous cell cancer
Rattus norvegicus (Norway rat)
DOID:0081381
  • juvenile amyotrophic lateral sclerosis type 27
Homo sapiens (human)
DOID:0050809
  • mucopolysaccharidosis IX
Danio rerio (zebrafish)
DOID:0060302
  • type II complement component 8 deficiency
Rattus norvegicus (Norway rat)
DOID:3996
  • urinary system cancer
Mus musculus (house mouse)
DOID:9631
  • Pelger-Huet anomaly
Mus musculus (house mouse)
DOID:0111428
  • essential tremor 1
  • Aliases:
    • ETM1
    • hereditary essential tremor 1
Mus musculus (house mouse)
DOID:12449
  • aplastic anemia
Caenorhabditis elegans
DOID:0111331
  • intellectual disability-severe speech delay-mild dysmorphism syndrome
  • Aliases:
    • FOXP1 Haploinsufficiency
    • FOXP1 syndrome
    • FOXP1-Related Neurodevelopmental Disorder
    • Mental retardation with language impairment and with or without autistic features
Mus musculus (house mouse)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Mus musculus (house mouse)
DOID:11199
  • hypoparathyroidism
Saccharomyces cerevisiae S288C
DOID:5463
  • cochlear disease
Mus musculus (house mouse)
DOID:0070509
  • Schinzel Giedion syndrome
  • Aliases:
    • SGS
    • Schinzel-Giedion midface retraction syndrome
Homo sapiens (human)
DOID:0060485
  • Mowat-Wilson syndrome
  • Aliases:
    • Hirschsprung disease mental retardation syndrome
    • microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease
Mus musculus (house mouse)
DOID:0070311
  • oligoasthenoteratozoospermia
  • Aliases:
    • OAT
    • oligoasthenoteratospermia
Mus musculus (house mouse)
DOID:526
  • human immunodeficiency virus infectious disease
  • Aliases:
    • HIV infection
Caenorhabditis elegans
DOID:1067
  • open-angle glaucoma
  • Aliases:
    • Wide-angle glaucoma
    • glaucoma simplex
    • open angle glaucoma
    • pigmentary glaucoma
Danio rerio (zebrafish)
DOID:3908
  • lung non-small cell carcinoma
  • Aliases:
    • NSCLC
    • Non-small cell lung cancer
    • non-small cell lung carcinoma
Xenopus laevis (African clawed frog)
DOID:2224
  • essential thrombocythemia
  • Aliases:
    • Essential thrombocythaemia
    • familial thrombocytosis
    • hemorrhagic thrombocythemia
    • hereditary thrombocythemia
    • primary Thrombocytosis
Caenorhabditis elegans
DOID:0110389
  • retinitis pigmentosa 73
  • Aliases:
    • RP73
Homo sapiens (human)
DOID:11870
  • Pick's disease
  • Aliases:
    • Dementia in Pick's disease
    • LOBAR ATROPHY OF BRAIN
    • PICK DISEASE OF BRAIN
    • Pick disease
Xenopus laevis (African clawed frog)
DOID:0112262
  • leucine-sensitive hypoglycemia of infancy
  • Aliases:
    • LIH
    • leucine-induced hypoglycemia
Rattus norvegicus (Norway rat)
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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