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 1001 - 1025 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:438
  • autoimmune disease of the nervous system
Homo sapiens (human)
DOID:417
  • autoimmune disease
  • Aliases:
    • autoimmune hypersensitivity disease
    • hypersensitivity reaction type II disease
Homo sapiens (human)
DOID:718
  • autoimmune hemolytic anemia
  • Aliases:
    • Autoimmune haemolytic anaemia
    • autoimmune hemolytic anaemia
Homo sapiens (human)
DOID:2048
  • autoimmune hepatitis
  • Aliases:
    • Autoimmune chronic active hepatitis
    • autoimmune hepatitis with centrilobular necrosis
Homo sapiens (human)
DOID:0110115
  • autoimmune lymphoproliferative syndrome type 2A
  • Aliases:
    • ALPS2A
    • autoimmune lymphoproliferative syndrome type IIA
Homo sapiens (human)
DOID:0110116
  • autoimmune lymphoproliferative syndrome type 2B
  • Aliases:
    • ALPS with recurrent viral infections
    • ALPS2B
    • CEDS
    • Caspase 8 deficiency
    • Caspase 8 deficiency syndrome
    • Caspase eight deficiency state
    • autoimmune lymphoproliferative syndrome type IIB
    • autoimmune lymphoproliferative syndrome with recurrent viral infections
Homo sapiens (human)
DOID:0110119
  • autoimmune lymphoproliferative syndrome type 3
  • Aliases:
    • ALPS3
    • autoimmune lymphoproliferative syndrome type III
Homo sapiens (human)
DOID:6688
  • autoimmune lymphoproliferative syndrome
  • Aliases:
    • ALPS
    • Canale-Smith syndrome
Homo sapiens (human)
DOID:0040091
  • autoimmune pancreatitis
Homo sapiens (human)
DOID:0050167
  • autoimmune polyendocrine syndrome type 1
  • Aliases:
    • Autoimmune Polyglandular Syndrome I
    • Whitaker syndrome
    • autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
Homo sapiens (human)
DOID:14040
  • autoimmune polyendocrine syndrome
  • Aliases:
    • Autoimmune polyglandular failure
    • Lloyd's syndrome
    • autoimmune polyendocrinopathy
Homo sapiens (human)
DOID:8924
  • autoimmune thrombocytopenic purpura
  • Aliases:
    • Immune thrombocytopenic purpura
    • idiopathic thrombocytopenic purpura
    • primary thrombocytopenic purpura
Homo sapiens (human)
DOID:7188
  • autoimmune thyroiditis
  • Aliases:
    • Chronic Lymphocytic Thyroiditis
    • Hashimoto thyroiditis
    • Hashimoto's Disease
    • Hashimoto's syndrome
    • Hashimoto's thyroiditis
    • Lymphocytic Thyroiditis
Homo sapiens (human)
DOID:11504
  • autonomic neuropathy
Homo sapiens (human)
DOID:0070247
  • autosomal dominant Emery-Dreifuss muscular dystrophy 2
  • Aliases:
    • EDMD2
    • EMD2
    • Emery-Dreifuss muscular dystrophy 2, autosomal dominant
    • Emery-Dreifuss muscular dystrophy, autosomal dominant
    • Hauptmann-Thannhauser muscular dystrophy
    • autosomal dominant limb-girdle muscular dystrophy type 1B
    • muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
    • scapuloilioperoneal atrophy with cardiopathy
Homo sapiens (human)
DOID:0060766
  • autosomal dominant Robinow syndrome 1
  • Aliases:
    • DRS1
Homo sapiens (human)
DOID:0060765
  • autosomal dominant Robinow syndrome 2
  • Aliases:
    • DRS2
Homo sapiens (human)
DOID:0060767
  • autosomal dominant Robinow syndrome 3
  • Aliases:
    • DRS3
Homo sapiens (human)
DOID:0060690
  • autosomal dominant auditory neuropathy 1
  • Aliases:
    • AUNA1
    • NSDAN
    • nonsyndromic dominant auditory neuropathy
Homo sapiens (human)
DOID:0111217
  • autosomal dominant centronuclear myopathy
  • Aliases:
    • AD-CNM
Homo sapiens (human)
DOID:1441
  • autosomal dominant cerebellar ataxia
  • Aliases:
    • spinocerebellar ataxia
Homo sapiens (human)
DOID:0060293
  • autosomal dominant chondrodysplasia punctata
Homo sapiens (human)
DOID:0070130
  • autosomal dominant cutis laxa 1
  • Aliases:
    • ADCL1
Homo sapiens (human)
DOID:0070136
  • autosomal dominant cutis laxa 2
  • Aliases:
    • ADCL2
Homo sapiens (human)
DOID:0070131
  • autosomal dominant cutis laxa 3
  • Aliases:
    • ADCL3
Homo sapiens (human)

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Last updated: August 19, 2024