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 1426 - 1450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0060230
  • basal ganglia calcification
  • Aliases:
    • Fahr disease
Drosophila melanogaster (fruit fly)
DOID:0060230
  • basal ganglia calcification
  • Aliases:
    • Fahr disease
Rattus norvegicus (Norway rat)
DOID:0060231
  • Bruck syndrome
  • Aliases:
    • osteogenesis imperfecta with congenital joint contractures
Drosophila melanogaster (fruit fly)
DOID:0060231
  • Bruck syndrome
  • Aliases:
    • osteogenesis imperfecta with congenital joint contractures
Mus musculus (house mouse)
DOID:0060233
  • cardiofaciocutaneous syndrome
  • Aliases:
    • CFC syndrome
    • cardio-facial-cutaneous syndrome
Mus musculus (house mouse)
DOID:0060233
  • cardiofaciocutaneous syndrome
  • Aliases:
    • CFC syndrome
    • cardio-facial-cutaneous syndrome
Homo sapiens (human)
DOID:0060234
  • Carpenter syndrome
  • Aliases:
    • acrocephalopolysyndactyly type II
Mus musculus (house mouse)
DOID:0060234
  • Carpenter syndrome
  • Aliases:
    • acrocephalopolysyndactyly type II
Homo sapiens (human)
DOID:0060237
  • Warburg micro syndrome
  • Aliases:
    • WARBM
    • Warburg-Sjo-Fledelius syndrome
    • micro syndrome
Mus musculus (house mouse)
DOID:0060239
  • Van der Woude syndrome
Mus musculus (house mouse)
DOID:0060240
  • UV-sensitive syndrome
Caenorhabditis elegans
DOID:0060240
  • UV-sensitive syndrome
Homo sapiens (human)
DOID:0060241
  • 3-M syndrome
  • Aliases:
    • Le Merrer syndrome
    • Miller-McKusick-Malvaux syndrome
    • Yakut short stature syndrome
    • dolichospondylic dysplasia
    • gloomy face syndrome
    • three M syndrome
Homo sapiens (human)
DOID:0060242
  • synpolydactyly
  • Aliases:
    • syndactyly type 2
Homo sapiens (human)
DOID:0060244
  • specific language impairment
Drosophila melanogaster (fruit fly)
DOID:0060244
  • specific language impairment
Mus musculus (house mouse)
DOID:0060244
  • specific language impairment
Caenorhabditis elegans
DOID:0060244
  • specific language impairment
Homo sapiens (human)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Rattus norvegicus (Norway rat)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Drosophila melanogaster (fruit fly)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Caenorhabditis elegans
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Mus musculus (house mouse)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Homo sapiens (human)
DOID:0060247
  • Smith-McCort dysplasia
Homo sapiens (human)
DOID:0060247
  • Smith-McCort dysplasia
Mus musculus (house mouse)

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Last updated: August 19, 2024