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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1176 - 1200 of 4621 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0080211
  • nodal marginal zone lymphoma
Homo sapiens (human)
DOID:8499
  • night blindness
  • Aliases:
    • nyctalopia
Homo sapiens (human)
DOID:0050742
  • nicotine dependence
  • Aliases:
    • tobacco use disorder
Homo sapiens (human)
DOID:12716
  • newborn respiratory distress syndrome
  • Aliases:
    • HMD - Hyaline membrane disease
    • Neonatal respiratory Distress syndrome
    • hyaline membrane disease
    • pulmonary hyaline membrane disease
    • pulmonary hypoperfusion syndrome of newborn
    • respiratory distress syndrome of newborn
Homo sapiens (human)
DOID:2512
  • nevoid basal cell carcinoma syndrome
  • Aliases:
    • Gorlin syndrome
    • NBCCS
    • basal cell nevus syndrome
Homo sapiens (human)
DOID:1227
  • neutropenia
Homo sapiens (human)
DOID:4964
  • neurotic disorder
  • Aliases:
    • Neurotic depression reactive type
    • Neurotic depressive state
    • Psychoneurosis
    • depressive neurosis
    • neurosis
    • neurotic depression
    • reactive depression
Homo sapiens (human)
DOID:870
  • neuropathy
  • Aliases:
    • peripheral neuropathy
Homo sapiens (human)
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Homo sapiens (human)
DOID:0110733
  • neuronal ceroid lipofuscinosis 9
  • Aliases:
    • CLN9
Homo sapiens (human)
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:0110722
  • neuronal ceroid lipofuscinosis 7
  • Aliases:
    • CLN7
Homo sapiens (human)
DOID:0110730
  • neuronal ceroid lipofuscinosis 6B
  • Aliases:
    • CLN4A
    • autosomal recessive neuronal ceroid lipofuscinosis 4A
    • neuronal ceroid lipofuscinosis 4A
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:0110728
  • neuronal ceroid lipofuscinosis 5
  • Aliases:
    • CLN5
    • neuronal ceroid lipofuscinosis 5 variable age of onset
Homo sapiens (human)
DOID:0110720
  • neuronal ceroid lipofuscinosis 4
  • Aliases:
    • CLN4B disease
    • autosomal dominant neuronal ceroid lipofuscinosis 4B
    • neuronal ceroid lipofuscinosis 4 Parry type
    • neuronal ceroid lipofuscinosis 4B
Homo sapiens (human)
DOID:0110731
  • neuronal ceroid lipofuscinosis 3
  • Aliases:
    • Batten disease
    • CLN3
    • juvenile neuronal ceroid lipofuscinosis
Homo sapiens (human)
DOID:0110726
  • neuronal ceroid lipofuscinosis 2
  • Aliases:
    • CLN2
    • neuronal ceroid lipofuscinosis 2 variable age at onset
Homo sapiens (human)
DOID:0110727
  • neuronal ceroid lipofuscinosis 13
  • Aliases:
    • CLN13
    • neuronal ceroid lipofuscinosis 13 Kufs type
Homo sapiens (human)
DOID:0110732
  • neuronal ceroid lipofuscinosis 11
  • Aliases:
    • CLN11
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:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Homo sapiens (human)
DOID:8869
  • neuromyelitis optica
  • Aliases:
    • Devic's disease
    • Devic's syndrome
Homo sapiens (human)
DOID:439
  • neuromuscular junction disease
Homo sapiens (human)

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Last updated: August 19, 2024