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 4601 - 4625 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:7426
  • cutaneous anthrax
Homo sapiens (human)
DOID:8295
  • scabies
  • Aliases:
    • Infestation by Sarcoptes scabiei
    • Infestation by Sarcoptes scabiei var hominis
    • Sarcoptic itch
Homo sapiens (human)
DOID:8478
  • actinomycosis
  • Aliases:
    • Actinomycotic madura foot
    • Actinomycotic mycetema
    • Actinomycotic mycetoma of foot
    • Madura foot due to Actinomadura
    • actinomycotic infection
Homo sapiens (human)
DOID:4346
  • variegate porphyria
  • Aliases:
    • Protocoproporphyria
    • Protoporphyrinogen oxidase deficiency
Homo sapiens (human)
DOID:14271
  • acute cholangitis
Homo sapiens (human)
DOID:14515
  • WAGR syndrome
  • Aliases:
    • 11p partial monosomy syndrome
    • Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome
    • chromosome 11p13 deletion syndrome
Homo sapiens (human)
DOID:4131
  • erythrasma
  • Aliases:
    • Infection due to Corynebacterium minutissimum
Homo sapiens (human)
DOID:14247
  • chronic purulent otitis media
  • Aliases:
    • chronic suppurative otitis media
Homo sapiens (human)
DOID:0060815
  • Miles-Carpenter syndrome
  • Aliases:
    • MCS
    • MRXS4
    • X-linked intellectual disability, Miles-Carpenter type
    • mental retardation, X-linked, syndromic 4
    • mental retardation, X-linked, with congenital contractures and low fingertip arches
Homo sapiens (human)
DOID:11506
  • suppurative otitis media
  • Aliases:
    • Otitis media with effusion - purulent
    • Purulent otitis media
Homo sapiens (human)
DOID:2582
  • acatalasia
  • Aliases:
    • acatalasemia
    • deficiency of catalase
Homo sapiens (human)
DOID:9767
  • myocardial stunning
Homo sapiens (human)
DOID:520
  • aortic disease
  • Aliases:
    • aortic disorder
    • disorder of the aorta
Homo sapiens (human)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Homo sapiens (human)
DOID:3301
  • gonadoblastoma
Homo sapiens (human)
DOID:0060451
  • Meesmann corneal dystrophy
  • Aliases:
    • MECD
    • Stocker-Holt dystrophy
    • juvenile hereditary epithelial dystrophy
Homo sapiens (human)
DOID:1787
  • pericarditis
Homo sapiens (human)
DOID:13507
  • trigonitis
Homo sapiens (human)
DOID:1679
  • cystitis
Homo sapiens (human)
DOID:2960
  • photosensitive trichothiodystrophy
  • Aliases:
    • IBIDS syndrome
    • TTD-P
    • Tay syndrome
    • sulfur-deficient brittle hair syndrome
    • trichothiodystrophy with congenital ichthyosis
Homo sapiens (human)
DOID:0081120
  • Graves ophthalmopathy
  • Aliases:
    • Graves orbitopathy
    • Thyroid associated ophthalmopathy
    • thyroid eye disease
Homo sapiens (human)
DOID:12287
  • Crimean-Congo hemorrhagic fever
  • Aliases:
    • CHF Congo virus
    • Congo-Crimean Hemorrhagic Fever
    • Crimean hemorrhagic fever
Homo sapiens (human)
DOID:0070145
  • hereditary sensory and autonomic neuropathy type 5
  • Aliases:
    • HSAN5
    • hereditary sensory and autonomic neuropathy type V
Homo sapiens (human)
DOID:161
  • keratosis
Homo sapiens (human)
DOID:10582
  • Refsum disease
  • Aliases:
    • HMSN type IV
    • HSMN IV
    • Heredopathia atactica polyneuritiformis
    • Refsum's disease
    • adult Refsum disease
    • classic Refsum disease
    • phytanic acid oxidase deficiency
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