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 351 - 375 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:7614
  • meninges sarcoma
  • Aliases:
    • Meningeal sarcoma
    • sarcoma of meninges
Homo sapiens (human)
DOID:12732
  • intermediate uveitis
  • Aliases:
    • chronic cyclitis
    • peripheral uveoretinitis
Homo sapiens (human)
DOID:10352
  • breast fibroadenosis
  • Aliases:
    • Fibroadenosis - breast
    • Fibroadenosis of breast
Homo sapiens (human)
DOID:0081292
  • traumatic brain injury
Homo sapiens (human)
DOID:11132
  • prostatic hypertrophy
Homo sapiens (human)
DOID:10242
  • ehrlichiosis
  • Aliases:
    • human ehrlichiosis
Homo sapiens (human)
DOID:0060158
  • acquired metabolic disease
Homo sapiens (human)
DOID:4291
  • fibroepithelial basal cell carcinoma
  • Aliases:
    • Fibroepithelioma of Pinkus
    • Fibroepithelioma of Pinkus type
    • Pinkus tumor
Homo sapiens (human)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Homo sapiens (human)
DOID:0060050
  • autoimmune disease of blood
Homo sapiens (human)
DOID:0060127
  • gamma heavy chain disease
  • Aliases:
    • Franklin's disease
Homo sapiens (human)
DOID:0060125
  • heavy chain disease
Homo sapiens (human)
DOID:8738
  • leukoplakia of penis
  • Aliases:
    • Kraurosis of penis
    • Penile Leukoplakia
Homo sapiens (human)
DOID:0080161
  • cutaneous candidiasis
Homo sapiens (human)
DOID:0060575
  • 3MC syndrome 1
Homo sapiens (human)
DOID:0060576
  • 3MC syndrome 2
Homo sapiens (human)
DOID:0050542
  • Charcot-Marie-Tooth disease type X
Homo sapiens (human)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Homo sapiens (human)
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Homo sapiens (human)
DOID:0080122
  • Alpers-Huttenlocher syndrome
  • Aliases:
    • Alper's syndrome
    • Alpers disease
    • Alpers progressive infantile poliodystrophy
    • Alpers syndrome
    • Alpers' disease or gray-matter degeneration
    • Diffuse Cerebral Sclerosis of Schilder
    • mitochondrial DNA depletion syndrome 4a
    • progressive sclerosing poliodystrophy
Homo sapiens (human)
DOID:3530
  • chronic wasting disease
Homo sapiens (human)
DOID:0060697
  • hyperekplexia 2
  • Aliases:
    • HKPX2
Homo sapiens (human)
DOID:5434
  • scrapie
Homo sapiens (human)
DOID:12170
  • radial nerve lesion
  • Aliases:
    • Lesion of radial nerve
    • Radial nerve lesions
Homo sapiens (human)
DOID:1442
  • obsolete Alpers syndrome
Homo sapiens (human)

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Last updated: August 19, 2024