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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 4201 - 4225 of 4649 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:3652
  • Leigh disease
  • Aliases:
    • Infantile necrotizing encephalomyelopathy
    • Leigh syndrome
    • juvenile subacute necrotizing encephalomyelopathy
Homo sapiens (human)
DOID:0070484
  • Legius syndrome
  • Aliases:
    • LGSS
    • NF1-like syndrome
    • neurofibromatosis type 1-like syndrome
Homo sapiens (human)
DOID:10457
  • Legionnaires' disease
  • Aliases:
    • Infection by Legionella pneumophilia
    • Legionella
    • Legionella pneumonia
    • Legionnaire's disease
Homo sapiens (human)
DOID:14415
  • Legg-Calve-Perthes disease
  • Aliases:
    • Calve - Perthes' disease
    • Coxa plana
    • Juvenile osteochond-hip/pelvis
    • Juvenile osteochondrosis of hip and/or pelvis
    • Perthe's disease
    • Perthes disease
    • juvenile osteochondrosis of hip and pelvis
    • osteochondrosis of Legg-Calve-Perthes
    • pseudocoxalgia
Homo sapiens (human)
DOID:705
  • Leber hereditary optic neuropathy
  • Aliases:
    • Leber's hereditary optic neuropathy
    • Leber's optic atrophy
Homo sapiens (human)
DOID:0111756
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
Homo sapiens (human)
DOID:14791
  • Leber congenital amaurosis
  • Aliases:
    • LCA
    • Leber's amaurosis
    • Leber's congenital amaurosis
    • Leber's disease
Homo sapiens (human)
DOID:0112240
  • Leber congenital amaurosis with early-onset deafness
  • Aliases:
    • LCAEOD
Homo sapiens (human)
DOID:0110079
  • Leber congenital amaurosis 8
  • Aliases:
    • LCA8
Homo sapiens (human)
DOID:0110217
  • Leber congenital amaurosis 17
  • Aliases:
    • LCA17
Homo sapiens (human)
DOID:0110078
  • Leber congenital amaurosis 1
  • Aliases:
    • LCA1
    • amaurosis congenita of Leber I
Homo sapiens (human)
DOID:1930
  • Laurence-Moon syndrome
  • Aliases:
    • LNMS
Homo sapiens (human)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Homo sapiens (human)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Homo sapiens (human)
DOID:9521
  • Laron syndrome
  • Aliases:
    • Laron-type isolated somatotropin defect
Homo sapiens (human)
DOID:0050214
  • Lambert-Eaton myasthenic syndrome
  • Aliases:
    • Eaton-Lambert syndrome
    • LEMS
    • Lambert-Eaton syndrome
Homo sapiens (human)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Homo sapiens (human)
DOID:0050574
  • L-2-hydroxyglutaric aciduria
  • Aliases:
    • L-2-HYDROXYGLUTARIC ACIDEMIA
Homo sapiens (human)
DOID:10873
  • Kuhnt-Junius degeneration
  • Aliases:
    • Exudative senile macular degeneration of retina
    • Neovascular age-related macular degeneration
    • Senile macular degeneration, wet
    • Wet senile macular retinal degeneration
Homo sapiens (human)
DOID:0060556
  • Kufor-Rakeb syndrome
  • Aliases:
    • autosomal recessive Parkinson disease 9
    • autosomal recessive juvenile onset Parkinson disease 9
Homo sapiens (human)
DOID:9597
  • Krukenberg carcinoma
  • Aliases:
    • Krukenberg neoplasm
Homo sapiens (human)
DOID:10587
  • Krabbe disease
  • Aliases:
    • Diffuse globoid body sclerosis
    • GLOBOID CELL LEUKOENCEPHALOPATHY
    • Galactosylceramide beta-galactosidase deficiency
    • Krabbe's disease
    • Krabbe's leukodystrophy
    • beta galactocerebrosidase deficiency
    • globoid cell leukodystrophy
Homo sapiens (human)
DOID:0050200
  • Korean hemorrhagic fever
Homo sapiens (human)
DOID:0050880
  • Koolen de Vries syndrome
  • Aliases:
    • 17q21.31 microdeletion syndrome
    • KANSL1-related intellectual disability syndrome
    • KdVS
    • Koolen-De Vries syndrome
Homo sapiens (human)
DOID:0111668
  • Kohlschutter-Tonz syndrome
  • Aliases:
    • KTZS
    • Kohlschutter's syndrome
    • amelocerebrohypohidrotic syndrome
    • epilepsy and yellow teeth
    • epilepsy dementia amelogenesis imperfecta
    • epilepsy-dementia-amelogenesis imperfecta syndrome
Homo sapiens (human)
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Last updated: February 17, 2025