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 2676 - 2700 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:1325
  • bronchus cancer
  • Aliases:
    • malignant neoplasm of bronchus and lung
    • malignant neoplasm of bronchus or lung
Homo sapiens (human)
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Drosophila melanogaster (fruit fly)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Homo sapiens (human)
DOID:0050073
  • invasive aspergillosis
Rattus norvegicus (Norway rat)
DOID:0110523
  • autosomal recessive nonsyndromic deafness 74
  • Aliases:
    • DFNB74
    • autosomal recessive deafness 74
Homo sapiens (human)
DOID:5854
  • silent myocardial infarction
Homo sapiens (human)
DOID:5492
  • biphasic synovial sarcoma
  • Aliases:
    • Biphasic sarcoma of Synovium
    • Synovial sarcoma, biphasic
Homo sapiens (human)
DOID:0090065
  • familial cold autoinflammatory syndrome 4
Homo sapiens (human)
DOID:4844
  • benign ependymoma
  • Aliases:
    • WHO grade II Ependymal tumor
    • epithelial ependymoma
Homo sapiens (human)
DOID:4977
  • lymphedema
  • Aliases:
    • Lymphatic edema
    • Lymphoedema
Homo sapiens (human)
DOID:0080557
  • congenital disorder of glycosylation Ie
  • Aliases:
    • congenital disorder of glycosylation 1e
Caenorhabditis elegans
DOID:1733
  • cryptosporidiosis
  • Aliases:
    • Cryptosporidial gastroenteritis
    • Infection by Cryptosporidium
    • intestinal cryptosporidiosis
Homo sapiens (human)
DOID:0070519
  • early-onset vitamin B6-dependent epilepsy 4
  • Aliases:
    • AASA dehydrogenase deficiency
    • EPEO4
    • PDE-ALDH7A1
    • antiquitin deficiency
Homo sapiens (human)
DOID:12930
  • dilated cardiomyopathy
  • Aliases:
    • primary dilated cardiomyopathy
Mus musculus (house mouse)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Homo sapiens (human)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
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
Rattus norvegicus (Norway rat)
DOID:9675
  • pulmonary emphysema
Rattus norvegicus (Norway rat)
DOID:10354
  • breast fibrocystic disease
  • Aliases:
    • Diffuse cystic mastopathy
    • Fibrocystic disease of breast
    • breast Fibrocystic Change
Homo sapiens (human)
DOID:12804
  • mucopolysaccharidosis IV
  • Aliases:
    • Mucopolysaccharidosis, MPS-IV
    • deficiency of N-acetylgalactosamine-6-sulphatase
    • deficiency of chondroitinsulphatase
    • galactosamine-6-sulfatase deficiency
Homo sapiens (human)
DOID:3321
  • GM2 gangliosidosis
  • Aliases:
    • gangliosidosis GM2
Mus musculus (house mouse)
DOID:319
  • spinal cord disease
Homo sapiens (human)
DOID:682
  • compartment syndrome
  • Aliases:
    • Compartmental syndrome
Homo sapiens (human)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Homo sapiens (human)
DOID:3118
  • hepatobiliary disease
  • Aliases:
    • liver and biliary tract 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