GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 251 - 275 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0080540
  • galactosialidosis
Caenorhabditis elegans
DOID:2378
  • relapsing-remitting multiple sclerosis
  • Aliases:
    • RRMS
    • Relapsing-remitting MS
Caenorhabditis elegans
DOID:0111042
  • glycogen storage disease IXa
  • Aliases:
    • GSD type 9A
    • GSD type IXa
    • GSD9A
    • glycogen storage disease type 9A
    • glycogen storage disease type IXa
    • glycogenosis type 9A
    • glycogenosis type IXa
Caenorhabditis elegans
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Caenorhabditis elegans
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Caenorhabditis elegans
DOID:9744
  • type 1 diabetes mellitus
  • Aliases:
    • IDDM
    • insulin-dependent diabetes mellitus
    • type I diabetes mellitus
Caenorhabditis elegans
DOID:0060643
  • primary sclerosing cholangitis
Caenorhabditis elegans
DOID:0112196
  • spondylometaepiphyseal dysplasia, short limb-hand type
  • Aliases:
    • SMED short limb-abnormal calcification type
    • SMED short limb-hand type
    • SMED type 2
    • SMED, type II
    • SMED-SL
    • SMED-SL/AC
    • spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
    • spondylometaepiphyseal dysplasia short limb-hand type
Caenorhabditis elegans
DOID:0070068
  • autosomal dominant intellectual developmental disorder 38
  • Aliases:
    • MRD38
    • PRELDS
    • autosomal dominant mental retardation 38
    • autosomal dominant non-syndromic intellectual disability 38
    • psychomotor retardation, epilepsy, and language disability syndrome
Caenorhabditis elegans
DOID:0050651
  • atrioventricular septal defect
  • Aliases:
    • AVCD
    • AVSD
    • ECD
    • atrioventricular canal defect
    • endocardial cushion defect
Caenorhabditis elegans
DOID:9784
  • trichinosis
  • Aliases:
    • Trichinella spiralis infection
Caenorhabditis elegans
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Caenorhabditis elegans
DOID:0080832
  • mild cognitive impairment
Caenorhabditis elegans
DOID:1679
  • cystitis
Caenorhabditis elegans
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Caenorhabditis elegans
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Caenorhabditis elegans
DOID:14261
  • fragile X syndrome
  • Aliases:
    • FRAGILE X MENTAL RETARDATION SYNDROME
    • MARKER X SYNDROME
    • MARTIN-BELL SYNDROME
Caenorhabditis elegans
DOID:13544
  • low tension glaucoma
  • Aliases:
    • Normal tension glaucoma
Caenorhabditis elegans
DOID:3635
  • congenital myasthenic syndrome
Caenorhabditis elegans
DOID:1508
  • candidiasis
  • Aliases:
    • Disseminated candidiasis
    • systemic candidiasis
Caenorhabditis elegans
DOID:1686
  • glaucoma
Caenorhabditis elegans
DOID:0080110
  • contractures, pterygia, and spondylocarpotarsal fusion syndrome
  • Aliases:
    • multiple pterygium syndrome
Caenorhabditis elegans
DOID:1909
  • melanoma
  • Aliases:
    • Naevocarcinoma
    • malignant melanoma
Caenorhabditis elegans
DOID:0070311
  • oligoasthenoteratozoospermia
  • Aliases:
    • OAT
    • oligoasthenoteratospermia
Caenorhabditis elegans
DOID:6652
  • diffuse idiopathic skeletal hyperostosis
  • Aliases:
    • Ankylosing vertebral hyperostosis
    • DISH
    • Disseminated idiopathic skeletal hyperostosis
Caenorhabditis elegans

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Last updated: December 9, 2024