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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 1351 - 1375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0111312
  • idiopathic generalized epilepsy 11
  • Aliases:
    • EIG11
Caenorhabditis elegans
DOID:0111265
  • Boucher-Neuhauser syndrome
  • Aliases:
    • ataxia-hypogonadism-choroidal dystrophy syndrome
Homo sapiens (human)
DOID:0110645
  • long QT syndrome 2
  • Aliases:
    • LQT2
Caenorhabditis elegans
DOID:10534
  • stomach cancer
  • Aliases:
    • gastric cancer
    • gastric neoplasm
Saccharomyces cerevisiae S288C
DOID:0080176
  • meningococcal meningitis
Drosophila melanogaster (fruit fly)
DOID:5520
  • head and neck squamous cell carcinoma
  • Aliases:
    • carcinoma of the head and neck
    • squamous cell carcinoma of the head and neck
    • squamous cell carcinomas of head and neck
Mus musculus (house mouse)
DOID:0110863
  • congenital stationary night blindness autosomal dominant 2
  • Aliases:
    • CSNBAD2
    • Rambusch type congenital stationary night blindness
Homo sapiens (human)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Drosophila melanogaster (fruit fly)
DOID:971
  • tendinitis
Mus musculus (house mouse)
DOID:3263
  • piebaldism
  • Aliases:
    • PIEBALD TRAIT
    • Partial albinism
Danio rerio (zebrafish)
DOID:0111460
  • cardiofaciocutaneous syndrome 1
  • Aliases:
    • CFC1
Mus musculus (house mouse)
DOID:2972
  • renal artery obstruction
Mus musculus (house mouse)
DOID:0110865
  • congenital stationary night blindness 1B
  • Aliases:
    • CSNB1B
    • autosomal recessive complete congenital stationary night blindness
    • congenital stationary night blindness 1B autosomal recessive
Homo sapiens (human)
DOID:1324
  • lung cancer
Xenopus tropicalis (tropical clawed frog)
DOID:0110345
  • osteogenesis imperfecta type 16
  • Aliases:
    • OI16
    • chromosome 11p11.2 deletion syndrome 91.3-KB
    • osteogenesis imperfecta type XVI
Rattus norvegicus (Norway rat)
DOID:0080444
  • developmental and epileptic encephalopathy 27
  • Aliases:
    • DEE27
    • early infantile epileptic encephalopathy 27
Mus musculus (house mouse)
DOID:9778
  • irritable bowel syndrome
  • Aliases:
    • IBD
    • Irritable colon
Danio rerio (zebrafish)
DOID:0111576
  • dehydrated hereditary stomatocytosis 1
  • Aliases:
    • PSHK1
    • dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema
    • pseudohyperkalemia edinburgh
    • pseudohyperkalemia familial 1, due to red cell leak
Mus musculus (house mouse)
DOID:0111265
  • Boucher-Neuhauser syndrome
  • Aliases:
    • ataxia-hypogonadism-choroidal dystrophy syndrome
Mus musculus (house mouse)
DOID:0110764
  • hereditary spastic paraplegia 11
  • Aliases:
    • HSP-TCC
    • Nakamura-Osame syndrome
    • SPG11
    • autosomal recessive spastic paraplegia 11
    • autosomal recessive spastic paraplegia complicated with thin corpus callosum
    • autosomal recessive spastic paraplegia type 11
    • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
    • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
Homo sapiens (human)
DOID:1441
  • autosomal dominant cerebellar ataxia
  • Aliases:
    • spinocerebellar ataxia
Homo sapiens (human)
DOID:0080728
  • Ehlers-Danlos syndrome arthrochalasia type 2
Mus musculus (house mouse)
DOID:0060464
  • Feingold syndrome
  • Aliases:
    • FGLDS
    • MODED syndrome
    • ODED syndrome
    • digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
    • microcephaly-digital anomalies-normal intelligence syndrome
    • microcephaly-oculo-digito-esophageal-duodenal syndrome
    • oculo-digito-esophageal-duodenal syndrome
Mus musculus (house mouse)
DOID:0070040
  • autosomal dominant intellectual developmental disorder 10
  • Aliases:
    • MRD10
    • autosomal dominant mental retardation 10
    • autosomal dominant non-syndromic intellectual disability 10
Homo sapiens (human)
DOID:0081042
  • T-cell prolymphocytic leukemia
  • Aliases:
    • Prolymphocytic leukemia, T-cell type
    • T Cell Prolymphocytic Leukemia
Homo sapiens (human)
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Last updated: December 9, 2024