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 3276 - 3300 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110787
  • hereditary spastic paraplegia 36
  • Aliases:
    • SPG36
    • autosomal dominant spastic paraplegia 36
    • autosomal dominant spastic paraplegia type 36
Homo sapiens (human)
DOID:1094
  • attention deficit hyperactivity disorder
  • Aliases:
    • ADHD
    • attention deficit disorder
    • hyperkinetic disorder
Homo sapiens (human)
DOID:0110254
  • cataract 25
  • Aliases:
    • CCSSO
    • CTRCT25
    • central pouch-like cataract with sutural opacities
    • central saccular cataract with sutural opacities
    • early-onset cataract with Y-shaped suture opacities
Homo sapiens (human)
DOID:0060580
  • Noonan syndrome 2
  • Aliases:
    • NS2
Homo sapiens (human)
DOID:10328
  • siderosis
  • Aliases:
    • pulmonary siderosis
Homo sapiens (human)
DOID:0110448
  • dilated cardiomyopathy 1HH
  • Aliases:
    • CMD1HH
Homo sapiens (human)
DOID:9245
  • Alagille syndrome
  • Aliases:
    • Alagille-Watson syndrome
    • Arteriohepatic dysplasia
Homo sapiens (human)
DOID:11486
  • Horner's syndrome
  • Aliases:
    • Bernard Horner syndrome
    • Horner syndrome
    • cervical sympathetic paralysis
Homo sapiens (human)
DOID:1686
  • glaucoma
Homo sapiens (human)
DOID:678
  • progressive supranuclear palsy
  • Aliases:
    • Steele-Richardson-Olszewski syndrome
    • progressive supranuclear ophthalmoplegia
Homo sapiens (human)
DOID:0050801
  • androgenic alopecia
  • Aliases:
    • alopecia androgenetica, male pattern baldness
    • androgenetic alopecia
Homo sapiens (human)
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Homo sapiens (human)
DOID:0070124
  • congenital nongoitrous hypothyroidism 2
  • Aliases:
    • CHNG2
    • congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
Homo sapiens (human)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Homo sapiens (human)
DOID:12842
  • Guillain-Barre syndrome
  • Aliases:
    • Infectious neuronitis
    • Post-infectious polyneuritis
    • Postinfectious polyneuritis
    • acute infective polyneuritis
    • acute inflammatory demyelinating polyradiculopathy
    • acute postinfectious polyneuropathy
Homo sapiens (human)
DOID:0080502
  • GM1 gangliosidosis type 1
Homo sapiens (human)
DOID:0060745
  • Doyne honeycomb retinal dystrophy
  • Aliases:
    • DHRD
    • Doyne honeycomb degeneration of retina
Homo sapiens (human)
DOID:0110592
  • autosomal dominant nonsyndromic deafness 70
  • Aliases:
    • DFNA70
    • autosomal dominant deafness 70
Homo sapiens (human)
DOID:9649
  • congenital nystagmus
Homo sapiens (human)
DOID:0060844
  • Norrie disease
  • Aliases:
    • Episkopi blindness
    • Norrie-Warburg disease
    • atrophia bulborum hereditaria
Homo sapiens (human)
DOID:10871
  • age related macular degeneration
  • Aliases:
    • Age Related Maculopathies
    • Age Related Maculopathy
    • Senile macular degeneration
    • Senile macular retinal degeneration
    • age-related macular degeneration
Homo sapiens (human)
DOID:3284
  • thymic carcinoma
  • Aliases:
    • Thymoma, malignant
    • malignant Thymoma
Homo sapiens (human)
DOID:5213
  • chronic inflammatory demyelinating polyradiculoneuropathy
Homo sapiens (human)
DOID:1073
  • renal hypertension
Homo sapiens (human)
DOID:11723
  • Duchenne muscular dystrophy
  • Aliases:
    • Muscular dystrophy, Duchenne
Homo sapiens (human)

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Last updated: August 19, 2024