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 2776 - 2800 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:1210
  • optic neuritis
Homo sapiens (human)
DOID:11650
  • bronchopulmonary dysplasia
  • Aliases:
    • Bronchopulmonary dysplasia of newborn
    • Chronic lung disease of prematurity
    • Neonatal chronic lung disease
    • Perinatal bronchopulmonary dysplasia
    • Respiratory insufficiency
    • neonatal chronic respiratory disease
Homo sapiens (human)
DOID:3720
  • extramedullary plasmacytoma
  • Aliases:
    • extraosseous plasmacytoma
    • plasmacytoma, extramedullary
Homo sapiens (human)
DOID:3275
  • thymoma
Homo sapiens (human)
DOID:3284
  • thymic carcinoma
  • Aliases:
    • Thymoma, malignant
    • malignant Thymoma
Homo sapiens (human)
DOID:874
  • bacterial pneumonia
  • Aliases:
    • Pneumonia due to other gram-negative bacteria
    • gram-negative pneumonia
Homo sapiens (human)
DOID:0111252
  • vestibular schwannomatosis
  • Aliases:
    • ACN
    • BANF
    • NF2
    • NF2-related schwannomatosis
    • SWN3
    • SWNV
    • acoustic neurofibromatosis
    • bilateral acoustic neurinoma
    • bilateral acoustic neurofibromatosis
    • bilateral acoustic schwannomas
    • central neurofibromatosis
    • familial acoustic neuromas
    • neurofibromatosis 2
    • neurofibromatosis type II
    • schwannomatosis 3
Homo sapiens (human)
DOID:4959
  • epidermolysis bullosa dystrophica
  • Aliases:
    • Dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:0060642
  • recessive dystrophic epidermolysis bullosa
  • Aliases:
    • RDEB, Hallopeau-Siemens type
    • autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
    • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
Homo sapiens (human)
DOID:11573
  • listeriosis
  • Aliases:
    • Infection by Listeria monocytogenes
    • Listeria infection
Homo sapiens (human)
DOID:4072
  • duodenum disease
  • Aliases:
    • duodenal disease
    • duodenum disorder
Homo sapiens (human)
DOID:0080217
  • lysosomal acid lipase deficiency
  • Aliases:
    • LAL deficiency
    • LAL-D
Homo sapiens (human)
DOID:3265
  • chronic granulomatous disease
  • Aliases:
    • Bridges-Good syndrome
    • CGD
    • Congenital dysphagocytosis
    • Quie syndrome
Homo sapiens (human)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Homo sapiens (human)
DOID:11446
  • sciatic neuropathy
Homo sapiens (human)
DOID:12043
  • kernicterus due to isoimmunization
Homo sapiens (human)
DOID:2382
  • kernicterus
  • Aliases:
    • bilirubin encephalopathy
Homo sapiens (human)
DOID:10323
  • byssinosis
  • Aliases:
    • Flax-dressers' disease
    • Stripper's asthma
    • cotton mill fever
Homo sapiens (human)
DOID:9201
  • lichen planus
  • Aliases:
    • Lichen, ruber planus
    • lichen ruber planus
Homo sapiens (human)
DOID:3108
  • ascaridiasis
Homo sapiens (human)
DOID:456
  • ascariasis
  • Aliases:
    • Ascariasis - roundworm
Homo sapiens (human)
DOID:12337
  • varicocele
  • Aliases:
    • Scrotal varices
Homo sapiens (human)
DOID:2565
  • macular corneal dystrophy
  • Aliases:
    • Fehr corneal dystrophy
    • MACULAR DYSTROPHY, CORNEAL, 1
Homo sapiens (human)
DOID:9111
  • cutaneous leishmaniasis
  • Aliases:
    • Asian Desert Cutaneous Leishmaniasis
    • Leproid leishmaniasis
    • diffuse cutaneous leishmaniasis
Homo sapiens (human)
DOID:9212
  • pityriasis rubra pilaris
  • Aliases:
    • Devergie's disease
Homo sapiens (human)

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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