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 4501 - 4525 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110300
  • obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
Homo sapiens (human)
DOID:13724
  • scurvy
Homo sapiens (human)
DOID:7213
  • transitional meningioma
  • Aliases:
    • transitional (mixed) meningioma
Homo sapiens (human)
DOID:14224
  • tracheal calcification
  • Aliases:
    • Calcification of trachea
Homo sapiens (human)
DOID:3108
  • ascaridiasis
Homo sapiens (human)
DOID:3664
  • mast cell neoplasm
  • Aliases:
    • Mast cell Proliferative disease
    • mast cell tumor
    • mastocytoma
Homo sapiens (human)
DOID:456
  • ascariasis
  • Aliases:
    • Ascariasis - roundworm
Homo sapiens (human)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Homo sapiens (human)
DOID:0110633
  • rigid spine muscular dystrophy 1
  • Aliases:
    • Eichsfeld type congenital muscular dystrophy
    • MDRS1
    • RSMD1
    • RSS
    • SEPN1-related myopathy
    • classic MmD
    • classic multiminicore disease
    • classic multiminicore myopathy
    • congenital merosin-positive muscular dystrophy with early spine rigidity
    • desmin-related myopathy with Mallory bodies
    • desmin-related myopathy with Mallory body-like inclusions
    • early-onset desmin-related myopathy
    • rigid spine syndrome
    • severe classic form minicore myopathy
    • severe classic form multicore myopathy
    • severe classic form multiminicore disease
Homo sapiens (human)
DOID:9643
  • babesiosis
  • Aliases:
    • Babesiasis
    • Infection by babesia
    • piroplasmosis
Homo sapiens (human)
DOID:0070268
  • congenital disorder of glycosylation type IIp
  • Aliases:
    • CDG IIp
    • CDG syndrome type IIp
    • CDG2P
    • CDGIIdp
    • Carbohydrate deficient glycoprotein syndrome type IIp
    • Congenital disorder of glycosylation type 2p
    • TMEM199-CDG
Homo sapiens (human)
DOID:2801
  • nonspecific interstitial pneumonia
  • Aliases:
    • NSIP
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:7997
  • thyrotoxicosis
Homo sapiens (human)
DOID:3137
  • obsolete multiple symmetrical lipomatosis
Homo sapiens (human)
DOID:11840
  • coronary artery vasospasm
  • Aliases:
    • Coronary Vasospasm
    • Coronary artery spasm
Homo sapiens (human)
DOID:1838
  • Menkes disease
  • Aliases:
    • COPPER TRANSPORT DISEASE
    • Menkes kinky-hair syndrome
    • steely hair syndrome
Homo sapiens (human)
DOID:203
  • exostosis
  • Aliases:
    • bone spur
    • bony outgrowth
    • orbital exostosis
    • osteophyte
    • swimmer's exostosis
Homo sapiens (human)
DOID:8691
  • mycosis fungoides
  • Aliases:
    • mycosis fungoides lymphoma
Homo sapiens (human)
DOID:0060768
  • Smith-Magenis syndrome
  • Aliases:
    • 17p11.2 microdeletion syndrome
    • chromosome 17p11.2 deletion syndrome
Homo sapiens (human)
DOID:0110307
  • hypertrophic cardiomyopathy 1
  • Aliases:
    • CMH1
    • cardiomyopathy, familial hypertrophic 1
    • hypertrophic cardiomyopathy 19
Homo sapiens (human)
DOID:0111058
  • platelet-type bleeding disorder 12
  • Aliases:
    • BDPLT12
    • PGHS1 deficiency
    • platelet COX1 deficiency
    • platelet cyclooxygenase 1 deficiency
    • platelet prostaglandin-endoperoxide synthase 1 deficiency
Homo sapiens (human)
DOID:7689
  • leptomeninges sarcoma
  • Aliases:
    • Leptomeningeal sarcoma
    • sarcoma of Leptomeninges
Homo sapiens (human)
DOID:11247
  • disseminated intravascular coagulation
  • Aliases:
    • DIC
    • Defibrination syndrome
    • Diffuse or disseminated intravascular coagulation
Homo sapiens (human)
DOID:4267
  • akinetic mutism
  • Aliases:
    • Coma vigilans
Homo sapiens (human)

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Last updated: August 19, 2024