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 2076 - 2100 of 4621 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:13133
  • HELLP syndrome
Homo sapiens (human)
DOID:13129
  • severe pre-eclampsia
  • Aliases:
    • Severe pre-eclampsia, with delivery
    • antepartum severe pre-eclampsia
    • postpartum severe pre-eclampsia
    • severe preeclampsia
Homo sapiens (human)
DOID:13121
  • deficiency anemia
  • Aliases:
    • deficiency anemias
Homo sapiens (human)
DOID:1312
  • focal segmental glomerulosclerosis
  • Aliases:
    • FGS
    • FSGS
    • focal glomerular sclerosis
    • focal glomerulosclerosis
Homo sapiens (human)
DOID:13100
  • intracranial vasospasm
Homo sapiens (human)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Homo sapiens (human)
DOID:13098
  • central retinal artery occlusion
Homo sapiens (human)
DOID:13097
  • intracranial arteriosclerosis
Homo sapiens (human)
DOID:13096
  • Sneddon syndrome
  • Aliases:
    • Idiopathic livedo reticularis with systemic involvement
Homo sapiens (human)
DOID:13094
  • branch retinal artery occlusion
  • Aliases:
    • Arterial retinal branch occlusion
    • retinal arterial branch occlusion
Homo sapiens (human)
DOID:13088
  • periventricular leukomalacia
Homo sapiens (human)
DOID:13087
  • Lown-Ganong-Levine syndrome
  • Aliases:
    • atrial tachyarrhythmia with short PR interval
    • syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias
Homo sapiens (human)
DOID:13078
  • eumycotic mycetoma
  • Aliases:
    • Madura foot
    • Maduromycosis, mycotic
    • Mycotic mycetoma
    • eumycetoma
    • maduromycosis
Homo sapiens (human)
DOID:13072
  • acquired hyperkeratosis
  • Aliases:
    • Keratoderma - acquired
    • Keratoderma, acquired
    • acquired keratoderma
Homo sapiens (human)
DOID:1307
  • dementia
Homo sapiens (human)
DOID:13068
  • renal osteodystrophy
  • Aliases:
    • renal rickets
Homo sapiens (human)
DOID:13042
  • persistent fetal circulation syndrome
  • Aliases:
    • Fetal circulation
    • Persistent fetal circulation
    • Persistent foetal circulation
    • congenital alveolar capillary dysplasia with misalignment of pulmonary veins
    • persistent foetal circulation syndrome
    • persistent pulmonary hypertension of the newborn
Homo sapiens (human)
DOID:13034
  • relapsing fever
Homo sapiens (human)
DOID:13025
  • retinopathy of prematurity
  • Aliases:
    • Retrolental fibroplasia
    • premature retinopathy
Homo sapiens (human)
DOID:13014
  • shipyard eye
  • Aliases:
    • EKC
    • Epidemic keratoconjunctivitis
Homo sapiens (human)
DOID:13003
  • vertebrobasilar insufficiency
  • Aliases:
    • Vertebro-basilar insufficiency
    • Vertebrobasilar arterial insufficiency
    • Vertebrobasilar artery syndrome
Homo sapiens (human)
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
DOID:12995
  • conduct disorder
Homo sapiens (human)
DOID:12987
  • agranulocytosis
  • Aliases:
    • Granulocytopenic disorder
    • Granulopenia
    • granulocytopenia
Homo sapiens (human)
DOID:12986
  • leukostasis
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