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 4551 - 4575 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:823
  • periapical periodontitis
  • Aliases:
    • Apical periodontitis
Homo sapiens (human)
DOID:11269
  • chronic apical periodontitis
Homo sapiens (human)
DOID:4617
  • periapical granuloma
  • Aliases:
    • Apical granuloma
Homo sapiens (human)
DOID:11573
  • listeriosis
  • Aliases:
    • Infection by Listeria monocytogenes
    • Listeria infection
Homo sapiens (human)
DOID:438
  • autoimmune disease of the nervous system
Homo sapiens (human)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Mus musculus (house mouse)
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Mus musculus (house mouse)
DOID:916
  • liver benign neoplasm
  • Aliases:
    • epithelial hepatic and intrahepatic bile duct neoplasm
Mus musculus (house mouse)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Mus musculus (house mouse)
DOID:0060198
  • amyotrophic lateral sclerosis type 6
  • Aliases:
    • ALS6
    • amyotrophic lateral sclerosis 6, with or without frontotemporal dementia
    • autosomal recessive amyotrophic lateral sclerosis 6
Homo sapiens (human)
DOID:4977
  • lymphedema
  • Aliases:
    • Lymphatic edema
    • Lymphoedema
Homo sapiens (human)
DOID:0070210
  • hereditary lymphedema IA
  • Aliases:
    • LMPH1A
Homo sapiens (human)
DOID:0070212
  • hereditary lymphedema I
  • Aliases:
    • LMPH1
    • Milroy disease
    • Nonne-Milroy lymphedema
    • PCL
    • congenital primary lymphedema
    • hereditary lymphedema type I
Homo sapiens (human)
DOID:0050580
  • hereditary lymphedema
Homo sapiens (human)
DOID:8791
  • breast carcinoma in situ
  • Aliases:
    • Non-Infiltrating carcinoma of breast
    • carcinoma in situ of breast
Homo sapiens (human)
DOID:3118
  • hepatobiliary disease
  • Aliases:
    • liver and biliary tract disease
Homo sapiens (human)
DOID:4976
  • elephantiasis
Homo sapiens (human)
DOID:0050775
  • schneckenbecken dysplasia
Homo sapiens (human)
DOID:0060465
  • fibrochondrogenesis
Homo sapiens (human)
DOID:0110220
  • Brugada syndrome 3
  • Aliases:
    • BRGDA3
Homo sapiens (human)
DOID:0110223
  • Brugada syndrome 6
  • Aliases:
    • BRGDA6
Homo sapiens (human)
DOID:0110224
  • Brugada syndrome 7
  • Aliases:
    • BRGDA7
Homo sapiens (human)
DOID:0110221
  • Brugada syndrome 4
  • Aliases:
    • BRGDA4
Homo sapiens (human)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Homo sapiens (human)
DOID:0110225
  • Brugada syndrome 8
  • Aliases:
    • BRGDA8
Homo sapiens (human)

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Last updated: August 19, 2024