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 2451 - 2475 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:0110847
  • xeroderma pigmentosum variant type
  • Aliases:
    • XPV
    • photosensitivity with defective DNA synthesis
    • xeroderma pigmentosum with normal DNA repair rates
Homo sapiens (human)
DOID:13778
  • chancroid
  • Aliases:
    • Ulcus molle, skin
Homo sapiens (human)
DOID:594
  • panic disorder
  • Aliases:
    • panic anxiety syndrome
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:5695
  • childhood liposarcoma
  • Aliases:
    • pediatric liposarcoma
Homo sapiens (human)
DOID:12359
  • endocrine exophthalmos
Homo sapiens (human)
DOID:0060692
  • platelet-type bleeding disorder 8
  • Aliases:
    • ADP platelet receptor P2Y12 defect
    • P2Y12 defect
Homo sapiens (human)
DOID:2411
  • granular cell tumor
  • Aliases:
    • neoplasm of granular cell
Homo sapiens (human)
DOID:3283
  • invasive malignant thymoma
  • Aliases:
    • Infiltrating Thymoma
    • Thymoma malignant Invasive
Homo sapiens (human)
DOID:0110636
  • congenital merosin-deficient muscular dystrophy 1A
  • Aliases:
    • CMD1A
    • MDC1A
    • Merosin-negative congenital muscular dystrophy
    • congenital muscular dystrophy due to laminin alpha2 deficiency
Homo sapiens (human)
DOID:1659
  • supratentorial cancer
  • Aliases:
    • Brain neoplasm, Supratentorial
    • malignant Supratentorial tumor
Homo sapiens (human)
DOID:11771
  • spontaneous ocular nystagmus
  • Aliases:
    • Ocular nystagmus
    • Searching eye movements
    • visual deprivation nystagmus
Homo sapiens (human)
DOID:14679
  • VACTERL association
Homo sapiens (human)
DOID:0050127
  • sinusitis
Homo sapiens (human)
DOID:9042
  • polyp of corpus uteri
  • Aliases:
    • endometrial/uterine polyp
    • polyp of Endometrium
    • polyp of the Uterus
    • polyp, uterus
Homo sapiens (human)
DOID:0070129
  • autosomal recessive cutis laxa type IID
  • Aliases:
    • ARCL2D
Homo sapiens (human)
DOID:0111054
  • von Willebrand's disease 3
  • Aliases:
    • VWD type 3
    • VWD3
    • von Willebrand disease type 3
    • von Willebrand disease type III
Homo sapiens (human)
DOID:0060171
  • obsolete Dravet syndrome
Homo sapiens (human)
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Homo sapiens (human)
DOID:986
  • alopecia areata
  • Aliases:
    • Circumscribed alopecia
Homo sapiens (human)
DOID:422
  • congenital structural myopathy
Homo sapiens (human)
DOID:10923
  • sickle cell anemia
  • Aliases:
    • Hb SC disease
    • Hb-S/Hb-C disease
    • Hb-SS disease without crisis
    • Hemoglobin S disease without crisis
    • Sickle-cell/Hb-C disease without crisis
    • drepanocytosis
    • haemoglobin SC disease
    • hemoglobin SC disease
    • sickle cell anaemia
Homo sapiens (human)
DOID:0060367
  • Parkinson's disease 1
  • Aliases:
    • autosomal dominant Parkinson disease 1
    • autosomal dominant Parkinson's disease 1
Homo sapiens (human)
DOID:0080073
  • spina bifida occulta
Homo sapiens (human)
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024