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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 7676 - 7700 of 15957 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111536
  • Buschke-Ollendorff syndrome
  • Aliases:
    • BOS
    • dermatofibrosis lenticularis disseminata with osteopoikilosis
    • dermatoosteopoikilosis
    • disseminated dermatofibrosis with osteopoikilosis
    • osteopathia condensans disseminata
Homo sapiens (human)
DOID:0111537
  • paroxysmal extreme pain disorder
  • Aliases:
    • PEPD
    • PEXPD
    • familial rectal pain
    • submandibular, ocular and rectal pain with flushing
Rattus norvegicus (Norway rat)
DOID:0111537
  • paroxysmal extreme pain disorder
  • Aliases:
    • PEPD
    • PEXPD
    • familial rectal pain
    • submandibular, ocular and rectal pain with flushing
Homo sapiens (human)
DOID:0111537
  • paroxysmal extreme pain disorder
  • Aliases:
    • PEPD
    • PEXPD
    • familial rectal pain
    • submandibular, ocular and rectal pain with flushing
Drosophila melanogaster (fruit fly)
DOID:0111538
  • paramyotonia congenita of Von Eulenburg
  • Aliases:
    • Eulenburg disease
    • PMC
    • Von Eulenburg paramyotonia congenita
    • myotonia congenita intermittens
    • paralysis periodica paramyotonica
    • paramyotonia congenita
Rattus norvegicus (Norway rat)
DOID:0111538
  • paramyotonia congenita of Von Eulenburg
  • Aliases:
    • Eulenburg disease
    • PMC
    • Von Eulenburg paramyotonia congenita
    • myotonia congenita intermittens
    • paralysis periodica paramyotonica
    • paramyotonia congenita
Mus musculus (house mouse)
DOID:0111538
  • paramyotonia congenita of Von Eulenburg
  • Aliases:
    • Eulenburg disease
    • PMC
    • Von Eulenburg paramyotonia congenita
    • myotonia congenita intermittens
    • paralysis periodica paramyotonica
    • paramyotonia congenita
Danio rerio (zebrafish)
DOID:0111538
  • paramyotonia congenita of Von Eulenburg
  • Aliases:
    • Eulenburg disease
    • PMC
    • Von Eulenburg paramyotonia congenita
    • myotonia congenita intermittens
    • paralysis periodica paramyotonica
    • paramyotonia congenita
Homo sapiens (human)
DOID:0111538
  • paramyotonia congenita of Von Eulenburg
  • Aliases:
    • Eulenburg disease
    • PMC
    • Von Eulenburg paramyotonia congenita
    • myotonia congenita intermittens
    • paralysis periodica paramyotonica
    • paramyotonia congenita
Drosophila melanogaster (fruit fly)
DOID:0111539
  • parastremmatic dwarfism
  • Aliases:
    • parastremmatic dysplasia
Mus musculus (house mouse)
DOID:0111541
  • pigmented paravenous chorioretinal atrophy
  • Aliases:
    • PPRCA
Homo sapiens (human)
DOID:0111541
  • pigmented paravenous chorioretinal atrophy
  • Aliases:
    • PPRCA
Mus musculus (house mouse)
DOID:0111541
  • pigmented paravenous chorioretinal atrophy
  • Aliases:
    • PPRCA
Drosophila melanogaster (fruit fly)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Homo sapiens (human)
DOID:0111542
  • familial expansile osteolysis
  • Aliases:
    • FEO
    • McCabe disease
    • hereditary expansile polyostotic osteolytic dysplasia
Mus musculus (house mouse)
DOID:0111543
  • juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
  • Aliases:
    • JP-HHT
Mus musculus (house mouse)
DOID:0111543
  • juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
  • Aliases:
    • JP-HHT
Homo sapiens (human)
DOID:0111545
  • familial male-limited precocious puberty
  • Aliases:
    • FMPP
    • familial gonadotropin-independent male-limited sexual precocity
    • male-limited precocious puberty
    • testotoxicosis
Homo sapiens (human)
DOID:0111545
  • familial male-limited precocious puberty
  • Aliases:
    • FMPP
    • familial gonadotropin-independent male-limited sexual precocity
    • male-limited precocious puberty
    • testotoxicosis
Mus musculus (house mouse)
DOID:0111545
  • familial male-limited precocious puberty
  • Aliases:
    • FMPP
    • familial gonadotropin-independent male-limited sexual precocity
    • male-limited precocious puberty
    • testotoxicosis
Rattus norvegicus (Norway rat)
DOID:0111546
  • Currarino syndrome
  • Aliases:
    • Currarino triad
Homo sapiens (human)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Homo sapiens (human)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Caenorhabditis elegans
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Mus musculus (house mouse)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Drosophila melanogaster (fruit fly)
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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: December 9, 2024