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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 2876 - 2900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:14793
  • hypohidrotic ectodermal dysplasia
Homo sapiens (human)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:299
  • adenocarcinoma
Xenopus tropicalis (tropical clawed frog)
DOID:438
  • autoimmune disease of the nervous system
Rattus norvegicus (Norway rat)
DOID:0050580
  • hereditary lymphedema
Drosophila melanogaster (fruit fly)
DOID:769
  • neuroblastoma
Rattus norvegicus (Norway rat)
DOID:0070316
  • Miura type epiphyseal chondrodysplasia
  • Aliases:
    • ECDM
    • tall stature-scoliosis-macrodactyly of the great toes syndrome
    • tall stature-scoliosis-macrodactyly of the halluces syndrome
Caenorhabditis elegans
DOID:0112383
  • KINSSHIP syndrome
  • Aliases:
    • AFF3-related mesomelic dysplasia
    • KINS
    • Steichen-Gersdorf type mesomelic dysplasia
Drosophila melanogaster (fruit fly)
DOID:1247
  • blood coagulation disease
  • Aliases:
    • coagulation protein disease
    • postpartum coagulation defect
    • postpartum coagulation defect with delivery
Mus musculus (house mouse)
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Drosophila melanogaster (fruit fly)
DOID:13576
  • twin-to-twin transfusion syndrome
  • Aliases:
    • Fetal blood loss from fetal hemorrhage into co-twin
    • Fetal hemorrhage into co-twin
    • Twin to twin transfusion
    • Twin-to-twin blood transfer
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Xenopus tropicalis (tropical clawed frog)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Mus musculus (house mouse)
DOID:0060341
  • agnathia-otocephaly complex
  • Aliases:
    • agnathia-holoprosencephaly-situs inversus syndrome
    • dysgnathia complex agnathia-holoprosencephaly
    • holoprosencephaly-agnathia
    • otocephaly
Homo sapiens (human)
DOID:12978
  • Plasmodium vivax malaria
  • Aliases:
    • Malaria by Plasmodium vivax
    • Vivax Malaria
Mus musculus (house mouse)
DOID:61
  • mitral valve disease
  • Aliases:
    • Mitral RH valve dis.
    • Rheumatic mitral insufficiency
    • Rheumatic mitral valve changes
    • Rheumatic mitral valve regurgitation
    • chronic rheumatic mitral valve
    • disease of mitral valve
    • rheumatic disease of mitral valve
    • rheumatic mitral valve incompetence
Danio rerio (zebrafish)
DOID:3210
  • Pelizaeus-Merzbacher disease
  • Aliases:
    • HLD1
    • Leukodystrophy, sudanophilic
    • PMD
    • Pelizaeus Merzbacher brain sclerosis
    • Pelizaeus-Merzbacher brain sclerosis
    • diffuse familial brain sclerosis
    • hypomyelinating leukodystrophy 1
    • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
Homo sapiens (human)
DOID:0080224
  • autosomal dominant dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0090102
  • autosomal dominant macrothrombocytopenia TUBB1-related
Homo sapiens (human)
DOID:321
  • tropical spastic paraparesis
  • Aliases:
    • HTLV-associated myelopathy
    • Tropical spastic paralysis
    • Tropical spastic paraplegia
Rattus norvegicus (Norway rat)
DOID:0110222
  • Brugada syndrome 5
  • Aliases:
    • BRGDA5
Mus musculus (house mouse)
DOID:0110859
  • polycystic kidney disease 2
  • Aliases:
    • Apkd2
    • Pkd2
    • Polycystic Kidney Disease, Adult, Type II
Danio rerio (zebrafish)
DOID:0112347
  • hereditary spastic paraplegia 84
  • Aliases:
    • SPG84
    • spastic paraplegia 84 autosomal recessive
Mus musculus (house mouse)
DOID:0080486
  • peroxisome biogenesis disorder 12A
  • Aliases:
    • peroxisome biogenesis disorder 12A (Zellweger)
Homo sapiens (human)
DOID:0080124
  • mitochondrial DNA depletion syndrome 5
  • Aliases:
    • succinate-CoA ligase deficiency
Homo sapiens (human)
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Last updated: December 9, 2024