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 2401 - 2425 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Mus musculus (house mouse)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Mus musculus (house mouse)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Mus musculus (house mouse)
DOID:12336
  • male infertility
Homo sapiens (human)
DOID:13922
  • eosinophilic esophagitis
Homo sapiens (human)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Homo sapiens (human)
DOID:4254
  • osteosclerosis
Homo sapiens (human)
DOID:0110946
  • autosomal recessive osteopetrosis 7
  • Aliases:
    • OPTB7
    • autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • autosomal recessive osteopetrosis type 7
    • osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • osteopetrosis-hypogammaglobulinemia syndrome
Homo sapiens (human)
DOID:0110938
  • autosomal dominant osteopetrosis 2
  • Aliases:
    • Albers-Schonberg osteopetrosis
    • OPTA2
    • autosomal dominant Albers-Schonberg disease
    • autosomal dominant osteopetrosis type II
    • osteopetrosis autosomal dominant type 2
Homo sapiens (human)
DOID:0050699
  • Dent disease
  • Aliases:
    • Dent disease 1
    • Dent disease 2
    • Dent's disease
Homo sapiens (human)
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Homo sapiens (human)
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Mus musculus (house mouse)
DOID:4762
  • vasculogenic impotence
Mus musculus (house mouse)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Mus musculus (house mouse)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Mus musculus (house mouse)
DOID:216
  • dental caries
  • Aliases:
    • Dental caries extending into pulp
    • Dental caries of smooth surface
    • Dental caries pit and fissure
Homo sapiens (human)
DOID:10461
  • dentin caries
  • Aliases:
    • Compound dental caries
    • Dental caries extending into dentine
Homo sapiens (human)
DOID:3770
  • pulmonary fibrosis
  • Aliases:
    • Fibrosis of lung
Mus musculus (house mouse)
DOID:0080855
  • Parkinsonism
Mus musculus (house mouse)
DOID:1459
  • hypothyroidism
  • Aliases:
    • Thyroid deficiency
    • Thyroid insufficiency
Mus musculus (house mouse)
DOID:11832
  • visual epilepsy
  • Aliases:
    • epilepsy, visual
Mus musculus (house mouse)
DOID:3525
  • middle cerebral artery infarction
Mus musculus (house mouse)
DOID:8398
  • osteoarthritis
  • Aliases:
    • Osteoarthrosis and allied disorder
    • degenerative arthritis
    • degenerative joint disease
    • hypertrophic arthritis
    • osteoarthrosis
Mus musculus (house mouse)
DOID:11132
  • prostatic hypertrophy
Mus musculus (house mouse)
DOID:4448
  • macular degeneration
  • Aliases:
    • Macular degeneration of retina
Mus musculus (house mouse)

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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