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 5601 - 5625 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Homo sapiens (human)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Homo sapiens (human)
DOID:0060560
  • lethal congenital contracture syndrome 2
  • Aliases:
    • LCCS2
    • multiple contracture syndrome, Israeli-Bedouin type
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Homo sapiens (human)
DOID:0060210
  • amyotrophic lateral sclerosis type 19
  • Aliases:
    • ALS19
    • amyotrophic lateral sclerosis 19
Homo sapiens (human)
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:0080913
  • cerebrooculofacioskeletal syndrome 3
Homo sapiens (human)
DOID:0110849
  • xeroderma pigmentosum group G
  • Aliases:
    • XP group G
    • XP7
    • XPG
    • xeroderma pigmentosum VII
Homo sapiens (human)
DOID:0080911
  • cerebrooculofacioskeletal syndrome 1
Homo sapiens (human)
DOID:14184
  • polyneuropathy due to drug
Homo sapiens (human)
DOID:0110028
  • age related macular degeneration 5
  • Aliases:
    • ARMD5
Homo sapiens (human)
DOID:0080908
  • Cockayne syndrome B
  • Aliases:
    • Cockayne syndrome 2
    • Cockayne syndrome type II
Homo sapiens (human)
DOID:0112158
  • De Sanctis-Cacchione syndrome
  • Aliases:
    • xeroderma pigmentosum with neurologic manifestation
Homo sapiens (human)
DOID:0060240
  • UV-sensitive syndrome
Homo sapiens (human)
DOID:0080868
  • primary ovarian insufficiency 11
Homo sapiens (human)
DOID:869
  • cholesteatoma
Homo sapiens (human)
DOID:0090124
  • neurogenic-type arthrogryposis multiplex congenita-2
  • Aliases:
    • AMC neurogenic type
    • AMC2
    • AMCN
    • arthrogryposis multiplex congenita 2, neurogenic type
    • arthrogryposis multiplex congenita neurogenic type
Homo sapiens (human)
DOID:0110813
  • hereditary spastic paraplegia 62
  • Aliases:
    • SPG62
    • autosomal recessive spastic paraplegia 62
    • autosomal recessive spastic paraplegia type 62
Homo sapiens (human)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Homo sapiens (human)
DOID:8557
  • oropharynx cancer
  • Aliases:
    • Oropharyngeal carcinoma
    • malignant Oropharyngeal tumor
    • malignant tumor of oropharynx
    • malignant tumour of mesopharynx
    • oropharyngeal cancer
Homo sapiens (human)
DOID:0070214
  • familial hyperinsulinemic hypoglycemia 7
  • Aliases:
    • EIHI
    • HHF7
    • exercise-induced hyperinsulinemic hypoglycemia
    • exercise-induced hyperinsulinism
    • hyperinsulinism due to SLC16A1 deficiency
    • hyperinsulinism due to monocarboxylate transporter 1 deficiency
Saccharomyces cerevisiae S288C
DOID:219
  • colon cancer
Saccharomyces cerevisiae S288C
DOID:326
  • ischemia
Saccharomyces cerevisiae S288C

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Last updated: December 9, 2024