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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 8576 - 8600 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0090015
  • Cenani-Lenz syndactyly syndrome
  • Aliases:
    • syndactyly type 7
Mus musculus (house mouse)
DOID:0110674
  • congenital myasthenic syndrome 17
  • Aliases:
    • CMS17
Mus musculus (house mouse)
DOID:0060757
  • sclerosteosis 2
  • Aliases:
    • SOST2
Mus musculus (house mouse)
DOID:12559
  • idiopathic juvenile osteoporosis
  • Aliases:
    • Idiopathic osteoporosis
    • juvenile osteoporosis
Mus musculus (house mouse)
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:0111411
  • exudative vitreoretinopathy 4
  • Aliases:
    • EVR4
Mus musculus (house mouse)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Mus musculus (house mouse)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Mus musculus (house mouse)
DOID:3652
  • Leigh disease
  • Aliases:
    • Infantile necrotizing encephalomyelopathy
    • Leigh syndrome
    • juvenile subacute necrotizing encephalomyelopathy
Mus musculus (house mouse)
DOID:0111180
  • French Canadian Leigh disease
  • Aliases:
    • French Canadian type COX deficiency
    • French Canadian type Leigh syndrome
    • French Canadian type cytochrome c oxidase deficiency
    • Saguenay Lac saint Jean type COX deficiency
    • Saguenay Lac saint Jean type Leigh syndrome
    • mitochondrial complex IV deficiency nuclear type 5
Mus musculus (house mouse)
DOID:0080588
  • agammaglobulinemia 5
Mus musculus (house mouse)
DOID:2583
  • agammaglobulinemia
  • Aliases:
    • IGHM
    • hypogammaglobulinemia
    • mu heavy chain deficiency
Rattus norvegicus (Norway rat)
DOID:0080588
  • agammaglobulinemia 5
Rattus norvegicus (Norway rat)
DOID:8505
  • dermatitis herpetiformis
  • Aliases:
    • Dermatosis herpetiformis
    • Duhring's disease
Mus musculus (house mouse)
DOID:4398
  • pustulosis of palm and sole
  • Aliases:
    • Acropustulosis
    • Palmoplantar Pustulosis
    • Pustular psoriasis of the palms and/or soles
Mus musculus (house mouse)
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Mus musculus (house mouse)
DOID:1024
  • leprosy
Rattus norvegicus (Norway rat)
DOID:8505
  • dermatitis herpetiformis
  • Aliases:
    • Dermatosis herpetiformis
    • Duhring's disease
Rattus norvegicus (Norway rat)
DOID:4398
  • pustulosis of palm and sole
  • Aliases:
    • Acropustulosis
    • Palmoplantar Pustulosis
    • Pustular psoriasis of the palms and/or soles
Rattus norvegicus (Norway rat)
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Rattus norvegicus (Norway rat)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Mus musculus (house mouse)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Rattus norvegicus (Norway rat)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Rattus norvegicus (Norway rat)
DOID:0111727
  • geleophysic dysplasia 3
  • Aliases:
    • GPHYSD3
Mus musculus (house mouse)
DOID:0090143
  • brachyolmia-amelogenesis imperfecta syndrome
  • Aliases:
    • DASS
    • STHAG6
    • dental anomalies and short stature
    • platyspondyly with amelogenesis imperfecta
    • selective tooth agenesis 5
Mus musculus (house mouse)
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Last updated: December 9, 2024