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 1301 - 1325 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Homo sapiens (human)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Mus musculus (house mouse)
DOID:0080038
  • pycnodysostosis
Homo sapiens (human)
DOID:0080041
  • hypochondroplasia
Homo sapiens (human)
DOID:0080046
  • Stickler syndrome
Homo sapiens (human)
DOID:0080047
  • pseudoachondroplasia
  • Aliases:
    • SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC
    • pseudoachondroplastic dysplasia
Drosophila melanogaster (fruit fly)
DOID:0080047
  • pseudoachondroplasia
  • Aliases:
    • SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC
    • pseudoachondroplastic dysplasia
Homo sapiens (human)
DOID:0080053
  • Albright's hereditary osteodystrophy
  • Aliases:
    • Albright hereditary osteodystrophy
    • pseudohypoparathyroidism type 1a
Homo sapiens (human)
DOID:0080055
  • achondrogenesis type IB
  • Aliases:
    • achondrogenesis Fraccaro type
Homo sapiens (human)
DOID:0080067
  • Charcot-Marie-Tooth disease type 5
  • Aliases:
    • hereditary motor and sensory neuropathy with pyramidal features
Homo sapiens (human)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Danio rerio (zebrafish)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Mus musculus (house mouse)
DOID:0080070
  • mucolipidosis II alpha/beta
  • Aliases:
    • I-cell disease
    • inclusion-cell disease
    • mucolipidosis II
Homo sapiens (human)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Mus musculus (house mouse)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Danio rerio (zebrafish)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Homo sapiens (human)
DOID:0080072
  • intestinal pseudo-obstruction
  • Aliases:
    • Chronic intestinal pseudo-obstruction
    • neuronal intestinal dysplasia
Homo sapiens (human)
DOID:0080073
  • spina bifida occulta
Homo sapiens (human)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Homo sapiens (human)
DOID:0080087
  • nonsyndromic congenital nail disorder 9
Homo sapiens (human)
DOID:0080089
  • tubular aggregate myopathy 1
Homo sapiens (human)
DOID:0080092
  • myofibrillar myopathy 1
  • Aliases:
    • autosomal recessive limb-girdle muscular dystrophy type 2R
    • desminopathy
Homo sapiens (human)
DOID:0080094
  • myofibrillar myopathy 3
  • Aliases:
    • LGMD 1A
    • autosomal dominant limb-girdle muscular dystrophy type 1A
    • myotilinopathy
    • spheroid body myopathy
Homo sapiens (human)
DOID:0080101
  • Compton-North congenital myopathy
  • Aliases:
    • congenital myopathy 12
Homo sapiens (human)
DOID:0080102
  • congenital myopathy 4A
  • Aliases:
    • CFTD
    • congenital fiber-type disproportion
Homo sapiens (human)

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Last updated: August 19, 2024