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 11826 - 11850 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Drosophila melanogaster (fruit fly)
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:0111411
  • exudative vitreoretinopathy 4
  • Aliases:
    • EVR4
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Homo sapiens (human)
DOID:12559
  • idiopathic juvenile osteoporosis
  • Aliases:
    • Idiopathic osteoporosis
    • juvenile osteoporosis
Homo sapiens (human)
DOID:83
  • cataract
Danio rerio (zebrafish)
DOID:10629
  • microphthalmia
  • Aliases:
    • microphthalmos
    • simple microphthalmos
Danio rerio (zebrafish)
DOID:0111432
  • essential tremor 5
  • Aliases:
    • ETM5
    • hereditary essential tremor 5
Drosophila melanogaster (fruit fly)
DOID:0080950
  • alopecia-mental retardation syndrome 4
Homo sapiens (human)
DOID:0110267
  • cataract 44
  • Aliases:
    • CTRCT44
    • total early-onset cataract
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Danio rerio (zebrafish)
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Homo sapiens (human)
DOID:4398
  • pustulosis of palm and sole
  • Aliases:
    • Acropustulosis
    • Palmoplantar Pustulosis
    • Pustular psoriasis of the palms and/or soles
Homo sapiens (human)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Homo sapiens (human)
DOID:0090143
  • brachyolmia-amelogenesis imperfecta syndrome
  • Aliases:
    • DASS
    • STHAG6
    • dental anomalies and short stature
    • platyspondyly with amelogenesis imperfecta
    • selective tooth agenesis 5
Homo sapiens (human)
DOID:0111727
  • geleophysic dysplasia 3
  • Aliases:
    • GPHYSD3
Homo sapiens (human)
DOID:5602
  • T-cell adult acute lymphocytic leukemia
  • Aliases:
    • ATLL
    • Acute Adult T-cell Leukemia-Lymphoma
    • adult Precursor T Lymphoblastic Leukemia
Drosophila melanogaster (fruit fly)
DOID:0111691
  • familial adult myoclonic epilepsy 5
  • Aliases:
    • FAME5
    • FCMTE5
    • familial cortical myoclonic tremor and epilepsy 5
Drosophila melanogaster (fruit fly)
DOID:0080101
  • Compton-North congenital myopathy
  • Aliases:
    • congenital myopathy 12
Drosophila melanogaster (fruit fly)
DOID:574
  • peripheral nervous system disease
Homo sapiens (human)
DOID:13689
  • prostate calculus
  • Aliases:
    • Prostatic lithiasis
    • Prostatic stone
    • Stone of prostate
    • calculus of prostate
Homo sapiens (human)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Homo sapiens (human)
DOID:14452
  • hypokalemic periodic paralysis
  • Aliases:
    • Hypokalemic familial periodic paralysis
    • Periodic paralysis I
    • Westphal disease
    • familial hypokalemic periodic paralysis
    • periodic hypokalemic paralysis
Danio rerio (zebrafish)

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Last updated: December 9, 2024