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 1076 - 1100 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0060890
  • ectopic Cushing syndrome
  • Aliases:
    • Cushing syndrome due to ectopic ACTH secretion
    • ectopic ACTH secreting tumor
Homo sapiens (human)
DOID:0060891
  • Parkinson's disease 19A
  • Aliases:
    • juvenile onset Parkinson disease 19A
    • juvenile onset Parkinson's disease 19A
Homo sapiens (human)
DOID:0060892
  • late onset Parkinson's disease
  • Aliases:
    • late onset Parkinson disease
Mus musculus (house mouse)
DOID:0060892
  • late onset Parkinson's disease
  • Aliases:
    • late onset Parkinson disease
Homo sapiens (human)
DOID:0060892
  • late onset Parkinson's disease
  • Aliases:
    • late onset Parkinson disease
Caenorhabditis elegans
DOID:0060894
  • early-onset Parkinson's disease
  • Aliases:
    • early-onset Parkinson disease
Homo sapiens (human)
DOID:0060895
  • Parkinson's disease 4
  • Aliases:
    • autosomal dominant Lewy body Parkinson disease 4
    • autosomal dominant Parkinson disease 4
    • autosomal dominant Parkinson's disease 4
Homo sapiens (human)
DOID:0060896
  • Parkinson's disease 23
  • Aliases:
    • autosomal recessive early-onset Parkinson disease 23
    • autosomal recessive early-onset Parkinson's disease 23
Homo sapiens (human)
DOID:0060898
  • Parkinson's disease 20
  • Aliases:
    • early-onset Parkinson disease 20
    • early-onset Parkinson's disease 20
Homo sapiens (human)
DOID:0060900
  • Parkinson's disease 14
  • Aliases:
    • Dystonia-Parkinsonism Adult-Onset
    • autosomal recessive Parkinson disease 14
    • autosomal recessive Parkinson's disease 14
Homo sapiens (human)
DOID:0060901
  • lymphoplasmacytic lymphoma
  • Aliases:
    • Waldenstroem's macroglobulinemia
    • Waldenstrom Macroglobulinemia
    • lymphoplasmacytic lymphoma with IgM gammopathy
Homo sapiens (human)
DOID:0060903
  • thrombosis
Homo sapiens (human)
DOID:0060911
  • karyomegalic interstitial nephritis
  • Aliases:
    • KIN
    • KMIN
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:0070014
  • autosomal dominant dyskeratosis congenita 1
  • Aliases:
    • DKCA1
    • Dyskeratosis Congenita, Scoggins Type
Homo sapiens (human)
DOID:0070025
  • X-linked dyskeratosis congenita
  • Aliases:
    • DKCX
    • Zinsser-Cole-Engman syndrome
Homo sapiens (human)
DOID:0070027
  • CST3-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis VI
    • Amyloidosis, Cerebroarterial, Icelandic Type
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
    • HCHWA
    • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Homo sapiens (human)
DOID:0070029
  • ITM2B-related cerebral amyloid angiopathy 1
  • Aliases:
    • Cerebral Amyloid Angiopathy, British Type
    • FBD
    • Familial British Dementia
    • Presenile Dementia with Spastic Ataxia
Homo sapiens (human)
DOID:0070030
  • ITM2B-related cerebral amyloid angiopathy 2
  • Aliases:
    • Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis
    • FDD
    • Familial Danish Dementia
    • HOOE
    • Heredopathia Ophthalmootoencephalica
Homo sapiens (human)
DOID:0070034
  • autosomal dominant intellectual developmental disorder 4
  • Aliases:
    • MRD4
    • autosomal dominant mental retardation 4
    • autosomal dominant non-syndromic intellectual disability 4
Homo sapiens (human)
DOID:0070042
  • Coffin-Siris syndrome 1
  • Aliases:
    • CSS1
    • MRD12
    • autosomal dominant mental retardation 12
    • fifth digit syndrome
Homo sapiens (human)
DOID:0070077
  • schizophrenia 1
  • Aliases:
    • SCZD1
Homo sapiens (human)
DOID:0070086
  • schizophrenia 10
  • Aliases:
    • SCZD10
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:0070111
  • Niemann-Pick disease type A
Caenorhabditis elegans

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Last updated: August 19, 2024