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 6476 - 6500 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0110723
  • neuronal ceroid lipofuscinosis 8
  • Aliases:
    • CLN8
Homo sapiens (human)
DOID:0110724
  • neuronal ceroid lipofuscinosis 8 northern epilepsy variant
  • Aliases:
    • EPMR
    • northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant
    • progressive epilepsy with mental retardation, northern epilepsy
    • progressive epilepsy-intellectual disability syndrome, Finnish type
Homo sapiens (human)
DOID:0110732
  • neuronal ceroid lipofuscinosis 11
  • Aliases:
    • CLN11
Homo sapiens (human)
DOID:0110727
  • neuronal ceroid lipofuscinosis 13
  • Aliases:
    • CLN13
    • neuronal ceroid lipofuscinosis 13 Kufs type
Homo sapiens (human)
DOID:0110731
  • neuronal ceroid lipofuscinosis 3
  • Aliases:
    • Batten disease
    • CLN3
    • juvenile neuronal ceroid lipofuscinosis
Homo sapiens (human)
DOID:0110722
  • neuronal ceroid lipofuscinosis 7
  • Aliases:
    • CLN7
Homo sapiens (human)
DOID:0110728
  • neuronal ceroid lipofuscinosis 5
  • Aliases:
    • CLN5
    • neuronal ceroid lipofuscinosis 5 variable age of onset
Homo sapiens (human)
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Homo sapiens (human)
DOID:0110729
  • neuronal ceroid lipofuscinosis 6A
  • Aliases:
    • CLN6
    • neuronal ceroid lipofuscinosis 6
    • neuronal ceroid lipofuscinosis 6 variable age of onset
Homo sapiens (human)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Homo sapiens (human)
DOID:3361
  • childhood osteosarcoma
  • Aliases:
    • pediatric osteosarcoma
Homo sapiens (human)
DOID:204
  • enthesopathy
Homo sapiens (human)
DOID:3376
  • bone osteosarcoma
  • Aliases:
    • Osteosarcoma of bone
    • primary Osteosarcoma of bone
Homo sapiens (human)
DOID:3347
  • osteosarcoma
  • Aliases:
    • Osteogenic sarcoma
    • Skeletal sarcoma
    • bone tissue neoplasm
    • osteoid sarcoma
Homo sapiens (human)
DOID:970
  • tenosynovitis
  • Aliases:
    • Inflammation of tendon sheath
Homo sapiens (human)
DOID:2703
  • synovitis
Homo sapiens (human)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Homo sapiens (human)
DOID:3429
  • inclusion body myositis
Homo sapiens (human)
DOID:4491
  • persian gulf syndrome
  • Aliases:
    • Gulf war syndrome
Homo sapiens (human)
DOID:3876
  • colonic pseudo-obstruction
  • Aliases:
    • primary chronic pseudo-obstruction of colon
Homo sapiens (human)
DOID:2163
  • nasal cavity disease
Homo sapiens (human)
DOID:0050161
  • lower respiratory tract disease
Homo sapiens (human)
DOID:4847
  • cauda equina neoplasm
  • Aliases:
    • tumor of the Cauda Equina
Homo sapiens (human)
DOID:0110667
  • congenital myasthenic syndrome 5
  • Aliases:
    • CMS Ic
    • CMS5
    • EAD
    • Engel congenital myasthenic syndrome
    • congenital myasthenic syndrome Engel type
    • congenital myasthenic syndrome type Ic
    • end plate acetylcholinesterase deficiency
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024